PRODIGESTAN perorálny prášok
PRODIGESTAN perorálny prášok
Authorised
- Sodium propionate
- Calcium propionate
- Manganese sulfate
- Copper sulfate pentahydrate
- Cobalt dichloride hexahydrate
- ZINC SULFATE HEPTAHYDRATE PH. EUR.
Product identification
Medicine name:
PRODIGESTAN perorálny prášok
Active substance:
- Sodium propionate
- Calcium propionate
- Manganese sulfate
- Copper sulfate pentahydrate
- Cobalt dichloride hexahydrate
- ZINC SULFATE HEPTAHYDRATE PH. EUR.
Target species:
-
Cattle
-
Sheep
-
Goat
-
Pig
-
Dog
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Sodium propionate506.60milligram(s)1.00gram(s)
-
Calcium propionate308.00milligram(s)1.00gram(s)
-
Manganese sulfate2.00milligram(s)1.00gram(s)
-
Copper sulfate pentahydrate1.00milligram(s)1.00gram(s)
-
Cobalt dichloride hexahydrate0.08milligram(s)1.00gram(s)
-
ZINC SULFATE HEPTAHYDRATE PH. EUR.0.08milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In drinking water use
- Cattle
- Sheep
- Goat
- Pig
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA16QA52
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
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:
- Tekro spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Tekro spol. s r.o.
Responsible authority:
- USKVBL
Authorisation number:
- 96/107/01-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 24/01/2022
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