Register
Medicines reference
Active substance

Carprofen

Propionic acid NSAID (COX-2 preferential). Registered in Georgia: 2 veterinary products. Forms: scored tablet, solution, tablet.

Dose and use

Doses

Each dose comes with its source. Check the label of the product you use.

Active substance Carprofen
Before use

Safety information

Known Contraindications

  • Critical
    Do not use carprofen in dogs with renal disease. Dehydration, hypovolaemia, or hypotension further increases the risk of renal toxicity.
    Sources: FDA
  • Critical
    Do not use carprofen in dogs with hepatic disease. Cyclooxygenase-inhibiting non-steroidal anti-inflammatory drugs can cause hepatic, renal, and gastrointestinal toxicity.
    Sources: FDA
  • Critical
    Do not use carprofen in animals with significant cardiac disease because haemodynamic compromise can increase renal and gastrointestinal risk.
  • Critical
    Do not use carprofen when gastrointestinal ulceration or bleeding is present or likely.
    Sources: FDA
  • Critical
    Do not use carprofen in patients with blood dyscrasia or a bleeding disorder.
    Sources: FDA
  • Critical
    Do not use carprofen during pregnancy or lactation. Fetotoxic effects occurred in laboratory animals at doses close to the therapeutic range.
    Sources: FDA
  • Critical
    Do not use carprofen during lactation. The injectable product is contraindicated during pregnancy and lactation in dogs and cats.
  • Critical
    Rimadyl should not be used in dogs exhibiting previous hypersensitivity to carprofen.
    Sources: FDA
  • Warning
    Avoid carprofen in dehydrated, hypovolaemic, or hypotensive dogs because renal toxicity may be increased.
  • Warning
    Do not use carprofen tablets in dogs younger than 4 months. Do not use the injectable product in dogs younger than 10 weeks or cats younger than 5 months.
    Sources: FDA
  • Warning (Cat)
    In cats, carprofen is limited to a single preoperative injection of 4 mg/kg. Do not repeat the injection and do not use oral carprofen products in cats.
    Sources: FDA

Known Drug Interactions

  • Contraindicated Carprofen + Robenacoxib
    Do not give robenacoxib together with other non-steroidal anti-inflammatory drugs or glucocorticoids because adverse gastrointestinal and renal effects may increase.
    Recommendation: Do not use these drugs together. Allow a treatment-free interval of at least 24 hours after the previous anti-inflammatory drug, extending it when required by that drug’s pharmacokinetics.
  • Major warning Meloxicam + Carprofen
    Do not give other non-steroidal anti-inflammatory drugs or glucocorticoids concurrently with carprofen or within 24 hours of treatment because gastrointestinal ulceration or perforation may occur.
    Recommendation: Consider appropriate washout times when switching from one NSAID to another or when switching from corticosteroid use to NSAID use.
    Sources: FDA
  • Major warning Carprofen + Dexamethasone
    Do not give other non-steroidal anti-inflammatory drugs or glucocorticoids concurrently with carprofen or within 24 hours of treatment because gastrointestinal ulceration or perforation may occur.
    Recommendation: Consider appropriate washout times when switching from one NSAID to another or when switching from corticosteroid use to NSAID use.
    Sources: FDA
  • Major warning Carprofen + Dihydrostreptomycin
    Avoid giving carprofen with potentially nephrotoxic drugs because renal toxicity may increase.
    Recommendation: Avoid concomitant use; if unavoidable, monitor renal function.
  • Major warning Carprofen + Prednisolone
    Do not give other non-steroidal anti-inflammatory drugs or glucocorticoids concurrently with carprofen or within 24 hours of treatment because gastrointestinal ulceration or perforation may occur.
    Recommendation: Consider appropriate washout times when switching from one NSAID to another or when switching from corticosteroid use to NSAID use.
    Sources: FDA
Latin name
Carprofen
Georgian name
კარპროფენი
Authorisation status
Authorised veterinary medicine
An authorised veterinary medicine containing this substance exists. Whether a particular use is on-label depends on the species and the indication - see each dose rule.
Registered in Georgia
2 of 4 forms
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026
All forms and registration4

Registration in Georgia and abroad: the register, number, validity and source are behind (i).

vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
5.1/10
Weak evidence support
vetman assessment

Artrin Plus

110/500/100/10 mg palatable scored tablets, N18 for dogs
Assessed clinical scopeDog · Full dog label from 3 kg: carprofen 110 mg with glucosamine, chondroitin and manganese for short courses of pain and inflammation in osteoarticular disease · oral
Care settingVeterinary-prescribed NSAID course after examination and risk screening, with weight-checked dosing
vetman score 5.1/10 Weak evidence support
Evidence confidence: Low Georgia: Yes, veterinary · № 000892 · Verified on 21 Oct 2026

A weak option: the carprofen works, but the coarse weight bands can roughly double the standard dose in small dogs and the added nutraceuticals bring no proven benefit. A single-agent, accurately dosed carprofen product is safer.

Regulatory and scientific credibility5.0/10

The N18 dog presentation is registered in Georgia (000892, valid to 2030) with the Argentine maker's leaflet; carprofen itself is EU-authorised for dogs with strong independent evidence, but this fixed combination has no EU, UK or US authorisation documented in the reviewed evidence or product study.

Clinical efficacy6.0/10

Carprofen reliably reduces osteoarthritis pain and inflammation in dogs; the glucosamine and chondroitin add no proven benefit, least of all over an 8-day course.

Safety and tolerability4.0/10

Weight bands give up to about 9 mg/kg carprofen at 3 kg and about 7 mg/kg at 8 kg, roughly double the usual 4 mg/kg daily dose; NSAID gastrointestinal, renal and hepatic risks apply and the leaflet leaves dose gaps at 7.5-8 kg and 15 kg.

Clinical practicality5.5/10

A palatable scored tablet once daily is easy to give, but quarter-tablet splitting and coarse bands make accurate dosing hard in small dogs.

Full-course cost-effectiveness-

No verified current Georgian price or patient-adjusted course cost was found; foreign prices were not substituted.

Important safety and use flags

  • Do not give to cats. Do not use in dogs with gastric ulcer, phenylketonuria or hypersensitivity to a component.
  • Weigh the dog: at the light end of each band the carprofen dose is well above 4 mg/kg (about 9 mg/kg at 3 kg); prefer an accurately dosed carprofen product in small dogs. No dose is set for 7.5-8 kg or exactly 15 kg.
  • Do not combine with other NSAIDs or glucocorticoids; allow a washout when switching.
  • Dehydration, renal, hepatic, cardiovascular or gastrointestinal disease, coagulation disorders, hypoproteinaemia and pregnancy need a benefit-risk decision before use.
  • Stop and seek veterinary advice for vomiting, dark stools, anorexia, lethargy, jaundice or changes in thirst or urination; check kidney and liver values in at-risk or older dogs.
Assessment sources
Assessed: 23 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Carprofen110 mg/tablet Glucosamine500 mg/tablet Chondroitin sulfate100 mg/tablet Manganese10 mg/tablet
Formulation Type
Scored tablet
Administration route
oral
Manufacturer
Brouwer S.A. · Argentina
Manufacturer (register)
BROUWER S.A, Argentina
Manufacturer and country as in the veterinary medicines register (National Food Agency), row 1436, 19 Oct 2026.
Registration
Georgia Yes, veterinary
In force until 14 Jul 2030
Veterinary (National Food Agency)
In the register: ართრინ პლუსი
№ 000892
Verified on: 21 Oct 2026
Controlled in Georgia
Unknown

Carprofen 50 mg, Tablet

tablet for dogs
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
Not rateable
No numerical score assigned
vetman assessment

Carprofen 50 mg

tablet for dogs
Assessed clinical scopeDog · Proposed oral treatment of canine musculoskeletal or degenerative-joint pain with the unidentified generic 50 mg carprofen tablet · By mouth
Care settingNot an established exact-product pathway; identify a marketed authorised carprofen product and use its own label before prescribing or calculating a dose
vetman score Not rateable No numerical score assigned
Evidence confidence: Low Georgia: Unknown · Verified on 22 Oct 2026 Off-label use
Not rateable

A numerical product score cannot responsibly be assigned. This row supplies only the generic name Carprofen 50 mg tablet for dogs and has no trade name, manufacturer or MA holder, authorisation number, pack, exact label or verified formulation. Its former EU, GB and US positive statuses named Rimadyl, Carprofen Orion or other products; its former Georgian negative statement was contradicted by the separately mapped, registered Rycarfa 50 mg presentation. Its 2-4 mg/kg dose, scored-tablet property and 24-hour half-tablet rule came from Rycarfa. Ingredient-level efficacy and safety evidence is strong, but it cannot establish this tablet’s legal status, quality, bioequivalence, excipients, palatability, subdivision, storage or dose delivery. Identify the exact product before scoring it.

Oral carprofen is a well-supported canine NSAID option for osteoarthritis and selected postoperative follow-up analgesia, but that favourable ingredient-level judgment belongs only to an identified, quality-controlled presentation. The catalogue must not turn a generic placeholder into Rycarfa or Rimadyl by inference.

Important safety and use flags

  • Exact product identity is missing. Do not infer manufacturer, authorisation, bioequivalence, excipients, meat flavour, equal subdivision, pack or quality from the generic catalogue name.
  • The 2-4 mg/kg Rycarfa regimen is comparator evidence, not this row’s product dose. The calculator is intentionally blocked until the marketed tablet is identified.
  • Dog only. Do not use oral carprofen tablets in cats; feline clearance and therapeutic margin differ, and current Rycarfa/Rimadyl tablet labels explicitly prohibit feline use.
  • Before treatment, obtain a thorough history and examination and consider baseline CBC, serum biochemistry and urinalysis. Reassess pain, function, hydration, blood pressure and renal/hepatic variables periodically, especially in older dogs or long courses.
  • Stop treatment and assess promptly for appetite loss, vomiting, diarrhoea, melena or hematemesis, lethargy, behaviour change, PU/PD, pallor, jaundice, ataxia, seizure, oedema or other suspected intolerance; rare serious or fatal reactions can occur without warning.
  • Do not combine with another NSAID or a glucocorticoid and do not give either within at least 24 hours of Rycarfa. Select any longer washout from the previous drug’s pharmacokinetics and the patient’s condition; use non-NSAID rescue analgesia if needed.
  • Avoid in dehydration, hypovolaemia or hypotension and in cardiac, hepatic or renal disease, gastrointestinal ulceration/bleeding risk or blood dyscrasia. Avoid potentially nephrotoxic drugs and closely review highly protein-bound or similarly metabolised medicines.
  • Do not use in pregnant or lactating bitches, dogs under 4 months, or patients hypersensitive to carprofen/NSAIDs or excipients. Use in aged dogs adds risk and requires careful management.
  • Scoring, crushing, flavour, storage and half-tablet stability are unverified for this generic row. Do not represent Rycarfa’s equal halves or 24-hour blister rule as its properties.
  • For chronic osteoarthritis, combine medicine with weight management, appropriate exercise/rehabilitation and other case-specific modalities. Reassess benefit regularly; carprofen controls pain and inflammation but does not modify the underlying joint disease.
Assessment sources
Assessed: 22 Oct 2026No axis or overall score is shown when the available evidence does not support a responsible numerical assessment.
Composition / strength
Carprofen50 mg
Formulation Type
Tablet
Administration route
By mouth
Manufacturer
-
Product
generic presentation, not registered in Georgia under a trade name
Registration
Georgia Unknown EU Not confirmed
Verified on: 22 Oct 2026
UK Not confirmed
Verified on: 22 Oct 2026
US Not confirmed
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

Carprofen 50 mg/ml, Solution

solution for injection for dogs and cats
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog Perioperative pain and inflammation using the listed injectable presentation
Not rateable
No numerical score assigned
vetman assessment

Carprofen 50 mg/ml

solution for injection for dogs and cats
Assessed clinical scopeDog · Perioperative pain and inflammation using the listed injectable presentation · SC,IV
Care settingVeterinary perioperative care after patient risk assessment, exact-product verification and multimodal analgesia planning
vetman score Not rateable No numerical score assigned
Evidence confidence: Medium Georgia: No · Verified on 22 Oct 2026 Off-label use
Not rateable

Injectable carprofen has strong canine regulatory and clinical evidence, but this catalogue row is not an exact product. It identifies no brand, manufacturer, MA number, sterile formulation/excipients, pack, storage instruction or pharmacovigilance endpoint. Rycarfa supports dog SC/IV perioperative use and Rimadyl supports dog SC use, but their labels differ and neither can be assigned to an anonymous row by ingredient and concentration alone.

Carprofen injection is evidence-based; the listed preparation is not identifiable. Map the row to a named, currently authorised or otherwise legally supplied product before assigning a product score or dose.

Important safety and use flags

  • This is a product-identity failure, not rejection of carprofen injection. Named authorised products and controlled trials support perioperative use, but their evidence cannot identify this anonymous row.
  • No brand, manufacturer, marketing-authorisation number, excipient formula, sterile pack, exact label, storage endpoint or pharmacovigilance contact is recorded. Do not select a label by matching only 50 mg/ml carprofen.
  • Rycarfa is SC/IV for dogs and cats; US Rimadyl is SC-only and dog-only. Verify the exact vial before choosing route, indication, repeat dose, storage or broached-vial life.
  • Do not publish 4 mg/kg as this anonymous product’s dose. Once a named applicable product is selected, follow its exact route/species label and use multimodal perioperative analgesia rather than treating one NSAID as the whole plan.
  • A named dog product may differ materially: Rycarfa permits IV/SC perioperative use and a possible half-dose top-up; Rimadyl is SC and also carries canine OA use. Do not combine labels.
  • Avoid use with cardiac, hepatic or renal disease, gastrointestinal ulceration/bleeding risk, major surgical blood loss, dehydration, hypovolaemia or hypotension. Establish history, examination and appropriate baseline laboratory data.
  • Do not combine with another NSAID or glucocorticoid and respect the exact label washout interval. Avoid potentially nephrotoxic drugs; high protein binding creates additional interaction risk.
  • Pregnancy and lactation safety is not established and current Rycarfa labelling prohibits use. Age limits are product-specific; current Rycarfa excludes dogs under 10 weeks and cats under 5 months.
  • Monitor for vomiting, diarrhoea, occult or visible blood, anorexia, lethargy, injection-site reaction and renal/hepatic injury. Stop and reassess promptly if an adverse sign appears.
  • Georgia has no current registered carprofen injection. EU/GB Rycarfa/Carprox and US Rimadyl are positive controls, not authorisations of this anonymous record; document the exact supplied vial and legal source.
Assessment sources
Assessed: 22 Oct 2026No axis or overall score is shown when the available evidence does not support a responsible numerical assessment.
Cat Single-dose perioperative pain control using the listed injectable presentation
Not rateable
No numerical score assigned
vetman assessment

Carprofen 50 mg/ml

solution for injection for dogs and cats
Assessed clinical scopeCat · Single-dose perioperative pain control using the listed injectable presentation · SC,IV
Care settingVeterinary perioperative care after patient risk assessment, exact-product verification and multimodal analgesia planning
vetman score Not rateable No numerical score assigned
Evidence confidence: Medium Georgia: No · Verified on 22 Oct 2026 Off-label use
Not rateable

A single 4 mg/kg perioperative carprofen injection has feline regulatory and controlled-trial support for named applicable products, but this catalogue row is not an exact product. It identifies no brand, manufacturer, MA number, sterile formulation/excipients, pack or label. This distinction is critical because current Rycarfa permits a single feline SC/IV dose while US Rimadyl explicitly prohibits cats. A numerical score would silently choose one unidentified formulation and legal endpoint.

Carprofen injection is evidence-based; the listed preparation is not identifiable. Map the row to a named, currently authorised or otherwise legally supplied product before assigning a product score or dose.

Important safety and use flags

  • This is a product-identity failure, not rejection of carprofen injection. Named authorised products and controlled trials support perioperative use, but their evidence cannot identify this anonymous row.
  • No brand, manufacturer, marketing-authorisation number, excipient formula, sterile pack, exact label, storage endpoint or pharmacovigilance contact is recorded. Do not select a label by matching only 50 mg/ml carprofen.
  • Feline use is formulation- and jurisdiction-specific. Rycarfa permits one perioperative SC/IV dose; US Rimadyl says do not use in cats. Never infer feline permission from concentration alone.
  • Do not publish 4 mg/kg as this anonymous product’s dose. Once a named applicable product is selected, follow its exact route/species label and use multimodal perioperative analgesia rather than treating one NSAID as the whole plan.
  • For a named product that authorises cats, the dose is single-use only: no repeat and no canine half-dose top-up. Cats have a longer, variable half-life and narrower therapeutic index.
  • Avoid use with cardiac, hepatic or renal disease, gastrointestinal ulceration/bleeding risk, major surgical blood loss, dehydration, hypovolaemia or hypotension. Establish history, examination and appropriate baseline laboratory data.
  • Do not combine with another NSAID or glucocorticoid and respect the exact label washout interval. Avoid potentially nephrotoxic drugs; high protein binding creates additional interaction risk.
  • Pregnancy and lactation safety is not established and current Rycarfa labelling prohibits use. Age limits are product-specific; current Rycarfa excludes dogs under 10 weeks and cats under 5 months.
  • Monitor for vomiting, diarrhoea, occult or visible blood, anorexia, lethargy, injection-site reaction and renal/hepatic injury. Stop and reassess promptly if an adverse sign appears.
  • Georgia has no current registered carprofen injection. EU/GB Rycarfa/Carprox and US Rimadyl are positive controls, not authorisations of this anonymous record; document the exact supplied vial and legal source.
Assessment sources
Assessed: 22 Oct 2026No axis or overall score is shown when the available evidence does not support a responsible numerical assessment.
Composition / strength
Carprofen50 mg/ml
Formulation Type
Solution
Administration route
Subcutaneous, Intravenous
Manufacturer
-
Product
generic presentation, not registered in Georgia under a trade name
Registration
Georgia No
EU Not confirmed
Verified on: 22 Oct 2026
UK Not confirmed
Verified on: 22 Oct 2026
US Not confirmed
Verified on: 22 Oct 2026
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026
Information not fully verified No dose is established for this exact anonymous preparation. Named Rycarfa 50 mg/ml has dog/cat SC/IV label doses; US Rimadyl 50 mg/ml is dog-only and SC-only. Do not transfer either label until brand, manufacturer, MA number, formulation, sterile pack and exact instructions are identified.

Rycarfa, Scored tablet

Carprofen 50 mg, meat-flavoured divisible tablet for dogs
vetman assessment
vetman’s 10-point assessment brings together a product’s regulatory credibility, clinical efficacy, safety and practicality. Cost-effectiveness is assessed only when reliable data are available. It is informational and does not replace a veterinarian’s clinical judgment for an individual patient.
Dog
8.0/10
Very good
vetman assessment

Rycarfa

Carprofen 50 mg, meat-flavoured divisible tablet for dogs
Assessed clinical scopeDog · Reduction of canine musculoskeletal and degenerative-joint pain and inflammation, plus up to five days of oral follow-up after parenteral preoperative analgesia · By mouth
Care settingVeterinary-directed home treatment after diagnosis and patient selection, with accurate weighing, response-guided dose reduction, toxicity counselling and periodic reassessment/monitoring
vetman score 8.0/10 Very good
Evidence confidence: High Georgia: Yes, veterinary · № 145-11; 232-11 · Verified on 19 Oct 2026

A well-documented, evidence-supported oral canine NSAID and a very good standard option for appropriately selected osteoarthritis patients, with useful short postoperative follow-up use. Its value depends on diagnosis, the lowest effective response-guided dose, multimodal care, baseline risk assessment and prompt withdrawal if intolerance appears; it is not for cats and not a harmless routine analgesic.

Regulatory and scientific credibility9.0/10

Exact Rycarfa 50 mg has current regulator-hosted EU/UK product information, a named MA holder, authorisation number, dog-only indications, complete dosing and safety text, and two current Georgian registrations. FDA-authorised oral carprofen products provide an additional mature regulatory and pharmacovigilance comparator.

Clinical efficacy8.5/10

Multiple placebo-controlled and active-comparator canine studies consistently support oral carprofen for osteoarthritis pain and function, and current pain guidelines place NSAIDs among core high-impact options. The evidence is strongest for OA; product-label postoperative follow-up is useful but is not a stand-alone multimodal perioperative plan or a disease-modifying claim.

Safety and tolerability6.5/10

Correctly selected dogs often tolerate carprofen well and controlled trials did not show a large routine toxicity signal, but the therapeutic margin is not trivial. Gastrointestinal ulceration/bleeding, renal injury, idiosyncratic hepatic injury and rare serious or fatal reactions remain clinically important; organ disease, dehydration, pregnancy/lactation, young age and interacting anti-inflammatory drugs materially narrow safe use.

Clinical practicality8.0/10

Meat flavour, once-daily use, optional division of the initial daily amount and equal half-tablets make home treatment workable. Accurate weight-based selection is still limited by 25 mg half-tablet increments; the unused half must return to the blister and be used within 24 hours, and long-term treatment requires regular clinical and laboratory review.

Full-course cost-effectiveness-

Price was not assessed and is excluded from the overall score.

Important safety and use flags

  • Verify exact Rycarfa 50 mg tablets for dogs. Do not transfer this score, half-tablet handling or dose to another carprofen brand, strength, chewable tablet, capsule or injection.
  • Weigh accurately. Give 2-4 mg/kg/day; the initial 4 mg/kg daily amount may be given once or split into two equal doses and may be reduced after 7 days to 2 mg/kg once daily according to response. Use the lowest effective dose.
  • Dog only. Do not use oral carprofen tablets in cats; feline clearance and therapeutic margin differ, and current Rycarfa/Rimadyl tablet labels explicitly prohibit feline use.
  • Before treatment, obtain a thorough history and examination and consider baseline CBC, serum biochemistry and urinalysis. Reassess pain, function, hydration, blood pressure and renal/hepatic variables periodically, especially in older dogs or long courses.
  • Stop treatment and assess promptly for appetite loss, vomiting, diarrhoea, melena or hematemesis, lethargy, behaviour change, PU/PD, pallor, jaundice, ataxia, seizure, oedema or other suspected intolerance; rare serious or fatal reactions can occur without warning.
  • Do not combine with another NSAID or a glucocorticoid and do not give either within at least 24 hours of Rycarfa. Select any longer washout from the previous drug’s pharmacokinetics and the patient’s condition; use non-NSAID rescue analgesia if needed.
  • Avoid in dehydration, hypovolaemia or hypotension and in cardiac, hepatic or renal disease, gastrointestinal ulceration/bleeding risk or blood dyscrasia. Avoid potentially nephrotoxic drugs and closely review highly protein-bound or similarly metabolised medicines.
  • Do not use in pregnant or lactating bitches, dogs under 4 months, or patients hypersensitive to carprofen/NSAIDs or excipients. Use in aged dogs adds risk and requires careful management.
  • The 50 mg tablet divides only into equal halves. Return the unused half to the opened blister, use it within 24 hours, protect from light/moisture and prevent accidental ingestion of the flavoured tablets.
  • For chronic osteoarthritis, combine medicine with weight management, appropriate exercise/rehabilitation and other case-specific modalities. Reassess benefit regularly; carprofen controls pain and inflammation but does not modify the underlying joint disease.
Assessment sources
Assessed: 22 Oct 2026The overall score uses 25/25/25/15/10 weights. An unassessed price is excluded and the remaining weights are proportionally renormalised.
Composition / strength
Carprofen50 mg
Formulation Type
Scored tablet
Administration route
By mouth
Manufacturer
Registration
Georgia Yes, veterinary
Controlled in Georgia
No
Checked against the narcotics law, Annex 1, lists I-IV, and Order No. 22/n.
Verified on: 16 Oct 2026

All of this shows in vetman as you prescribe

The dose for the patient's weight, registration in Georgia and controlled status, right on the prescription.