Sulfadimethoxine

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This page reprints a manufacturer label. Everything below in quotation marks is copied from ALBON ® (sulfadimethoxine), published by FDA and retrieved on 2026-09-16. Nothing has been added, reworded or left out of the sections shown. It is the manufacturer’s label, reproduced as published.

This page reprints the FDA label for ALBON ® (sulfadimethoxine) by Zoetis Inc, a sulfadimethoxine product labelled for dogs and cats. The sections below are copied from that label without change, with the set id and the date it was retrieved from DailyMed. 1 other stored label carries the same active ingredient and is listed at the end.

The label

Product: ALBON ® (sulfadimethoxine). Manufacturer: Zoetis Inc. FDA Structured Product Label set id 24094a36-0c38-4af1-b9ab-b4b12f342e33. Label effective 2019-11-07. Retrieved 2026-09-16 from the DailyMed animal label release, and readable on DailyMed.

Indications

Albon is indicated for the treatment of respiratory, genitourinary tract, enteric, and soft tissue infections in dogs and cats: tonsillitis pharyngitis bronchitis pneumonia cystitis nephritis metritis pyometra pustular dermatitis anal gland infections abscesses wound infections bacterial enteritis canine salmonellosis bacterial enteritis associated with coccidiosis in dogs when caused by streptococci, staphylococci, escherichia, salmonella, klebsiella, proteus or shigella organisms sensitive to sulfadimethoxine. Limitations: Sulfadimethoxine is not effective in viral or rickettsial infections, and as with any antibacterial agent, occasional failures in therapy may occur due to resistant microorganisms. The usual precautions in sulfonamide therapy should be observed.

Dosage and Administration

Initial Dose: 25 mg/lb (55 mg/kg) of animal body weight. Subsequent Daily Doses: 12.5 mg/lb (27.5 mg/kg) of animal body weight. Dogs and cats should receive 1 teaspoonful of Albon Oral Suspension 5% per 10 lb of body weight (25 mg/lb or 55 mg/kg) as an initial dose, followed by 1/2 teaspoonful per 10 lb of body weight (12.5 mg/lb or 27.5 mg/kg) every 24 hours thereafter. Representative weights and doses are indicated in the following table: Animal Weight Initial Dose 25 mg/lb (55 mg/kg) Subsequent Daily Doses 12.5 mg/lb (27.5 mg/kg) 5 lb (2.2 kg) 1/2 tsp (2 1/2 mL) 1/4 tsp (1 1/4 mL) 10 lb (4.5 kg) 1 tsp (5 mL) 1/2 tsp (2 1/2 mL) 20 lb (9.1 kg) 2 tsp (10 mL) 1 tsp (5 mL) 40 lb (18.2 kg) 4 tsp (20 mL) 2 tsp (10 mL) 80 lb (36.4 kg) 8 tsp (40 mL) 4 tsp (20 mL) Treatment may be initiated with Albon Injection 40% to obtain effective blood levels almost immediately or to facilitate treatment of the fractious animal. Length of treatment depends on the clinical response. In most cases treatment for 3–5 days is adequate. Treatment should be continued until the animal is asymptomatic for 48 hours. TOXICITY AND SAFETY Data regarding acute and chronic toxicities of sulfadimethoxine indicate the drug is very safe. The LD 50 in mice is greater than 2 g/kg of body weight when administered intraperitoneally and greater than 16 g/kg when administered orally. In dogs receiving massive single oral doses of 3.2 g/kg of body weight, diarrhea was the only adverse effect observed. Dogs given 160 mg/kg of body weight orally daily for 13 weeks showed no signs of toxicity.

Precautions

During treatment period, make certain that animals maintain adequate water intake. If animals show no improvement within 2 or 3 days, reevaluate your diagnosis.

Description

Albon is a low-dosage, rapidly absorbed, long-acting sulfonamide, effective for the treatment of a wide range of bacterial infections commonly encountered in dogs and cats. Sulfadimethoxine is a white, almost tasteless and odorless compound. Chemically, it is N 1 -(2,6-dimethoxy-4-pyrimidinyl) sulfanilamide. The structural formula is: Chemical Structure

Storage

Store at controlled room temperature 15°–30°C (59°–86°F).

Other labels for this ingredient

These labels are also stored for the same active ingredient. They are not identical to the one reprinted above, and each is listed by product and set id rather than merged with it.

FDA adverse event reports

The FDA Center for Veterinary Medicine publishes the adverse event reports it receives through openFDA. The counts below are the reports naming sulfadimethoxine as an active ingredient for each species this label names, as returned on 2026-09-16, coded by the VeDDRA reaction term the reporter chose. Reactions are counted per report, so one report can appear under several terms.

These are counts, not rates. Reporting is voluntary, the number of animals treated is not known, and a widely used product accumulates reports for that reason alone. A report records that an event followed a dose; it does not establish that the product caused it. The counts say nothing about how one product compares with another.

Dogs: 1,949 reports

Reactions most often coded in dogs, 1,949 reports
VeDDRA reaction termReports
Vomiting293
Depression239
Anorexia197
Lack of efficacy (protozoa) - Coccidia172
Fever168
Death154
Diarrhoea154
Ataxia150
Anaemia NOS115
Convulsion115
Elevated serum alkaline phosphatase (SAP)109
Lethargy (see also Central nervous system depression in 'Neurological')109
Thrombocytopenia109
Elevated alanine aminotransferase (ALT)105
Death by euthanasia83

Outcome as recorded by the reporter: Ongoing 239; Died 221; Recovered/Normal 162; Outcome Unknown 118; Euthanized 24; Recovered with Sequela 6.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Cats: 360 reports

Reactions most often coded in cats, 360 reports
VeDDRA reaction termReports
Lack of efficacy (protozoa) - Coccidia125
Diarrhoea50
Death40
Vomiting39
Depression30
Fever29
Anorexia27
Ataxia20
Death by euthanasia17
Anaemia NOS16
Lethargy (see also Central nervous system depression in 'Neurological')16
No sign15
Hypersalivation14
Convulsion13
Dehydration13

Outcome as recorded by the reporter: Died 56; Ongoing 47; Outcome Unknown 40; Recovered/Normal 14; Euthanized 2; Recovered with Sequela 1.

Queries: reports, reactions, outcomes. Dataset: openFDA Animal and Veterinary Adverse Event Reports.

Sources

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