Alamycin, 32,1 mg/g nahasprei, lahus veistele, lammastele ja sigadele.
Alamycin, 32,1 mg/g nahasprei, lahus veistele, lammastele ja sigadele.
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Alamycin, 32,1 mg/g nahasprei, lahus veistele, lammastele ja sigadele.
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride36.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Cutaneous spray, solution
Withdrawal period by route of administration:
-
Cutaneous use
- Cattle
-
Meat and offal0day
-
Milk0dayMitte kasutada lakteerivate loomade udaral ega nisadel, kui nende piima tarvitatakse inimtoiduks.
-
- Sheep
-
Meat and offal0day
-
Milk0dayMitte kasutada lakteerivate loomade udaral ega nisadel, kui nende piima tarvitatakse inimtoiduks.
-
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Estonia
Package description:
- Available only in Estonian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Manufacturing Limited
- Norbrook Laboratories Limited
Responsible authority:
- State Agency Of Medicines
Authorisation number:
- 1199
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
This document does not exist in this language (English). You can find it in another language below.
Estonian (PDF)
Published on: 26/01/2022
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