Albendazole — Active Pharmaceutical Ingredient

Albendazole is an active pharmaceutical ingredient found in 2 FDA-approved drug products. Forms: TABLET. Routes: ORAL.

This content is for informational purposes only. Always consult a healthcare professional.

Albendazole (2 brand names, 1 dosage form, 1 route)

Available dosage forms: TABLET.

Routes of administration: ORAL.

Brand Names

  • ALBENDAZOLE
  • ALBENZA

Dosage and Administration

Albendamax Suspension should be administered to cattle and goats at the recommended rate of 4 mL/100 lb of body weight (equivalent to 4.54 mg of albendazole/lb, 10 mg/kg) and to sheep at the recommended rate of 0.75 mL/25 lb of body weight (equivalent to 3.4 mg of albendazole/lb, 7.5 mg/kg). Do not underdose. Ensure each animal receives a complete dose based on a current body weight. Underdosing may result in ineffective treatment, and encourage the development of parasite resistance. NOT FOR HUMAN USE. KEEP AWAY FROM CHILDREN. Use only as directed.

Warnings and Precautions

Important Accurate estimates of the weight of the cattle, sheep, and goats to be treated are essential for effective results. Animals consistently exposed to internal parasites should be retreated as necessary. Residue Warnings Cattle must not be slaughtered within 27 days following last treatment. Sheep and Goats must not be slaughtered within 7 days following last treatment. A withdrawal time in milk has not been established; Do not use in female breeding dairy cattle. Do not use in lactating female sheep or goats. Other Warnings Parasite resistance may develop to any dewormer, and has been reported for most classes of dewormers. Treatment with a dewormers AND parasite management practices appropriate to the region and the animal(s) treated may slow the development of parasite resistance. Fecal examinations or other diagnostic tests should be used to determine if this product is appropriate, prior to the use of any dewormer. Following the use of any dewormer, effectiveness of treatment should be monitored, e.g., fecal egg count reduction test. A decrease in a drug’s effectiveness over time as calculated by fecal egg count reduction tests may indicate the development of resistance to the dewormer administered. Your parasite management plan should be adjusted accordingly. Precaution Do not administer to female cattle during first 45 days of pregnancy or for 45 days after removal of bulls. Do not administer to ewes or does during the first 30 days of pregnancy or for 30 days after removal of rams or bucks. Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.