ALBENDAZOL 300 mg, 600 mg and 1200 mg
ALBENDAZOL 300 mg, 600 mg and 1200 mg
Authorised
- Albendazole
- Albendazole
- Albendazole
Product identification
Medicine name:
ALBENDAZOL 300 mg, 600 mg and 1200 mg
Active substance:
- Albendazole
- Albendazole
- Albendazole
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Albendazole1200.00/milligram(s)1.00Tablet
-
Albendazole600.00/milligram(s)1.00Tablet
-
Albendazole300.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal14day
-
Milk72hourмляко - 72 часа след последното третиране
-
-
Sheep
-
Meat and offal7dayмляко - не се разрешава за употреба при овце, чието мляко е предназначено за консумация от хора
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC11
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Farma Sis OOD
Marketing authorisation date:
Manufacturing sites for batch release:
- Golash Pharma OOD
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1971
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Bulgarian (PDF)
Published on: 30/05/2022