Combivit (35 mg + 0,5 mg + 7 mg + 23 mg + 70 mg)/ml Roztwór do wstrzykiwań
Combivit (35 mg + 0,5 mg + 7 mg + 23 mg + 70 mg)/ml Roztwór do wstrzykiwań
Authorised
- Ascorbic acid
- Thiamine
- Pyridoxine hydrochloride
- Riboflavin
- Nicotinamide
Product identification
Medicine name:
Combivit (35 mg + 0,5 mg + 7 mg + 23 mg + 70 mg)/ml Roztwór do wstrzykiwań
Active substance:
- Ascorbic acid
- Thiamine
- Pyridoxine hydrochloride
- Riboflavin
- Nicotinamide
Target species:
-
Cat
-
Dog
-
Horse
-
Goat
-
Pig
-
Cattle
-
Sheep
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Ascorbic acid70.00milligram(s)1.00millilitre(s)
-
Thiamine35.00milligram(s)1.00millilitre(s)
-
Pyridoxine hydrochloride7.00milligram(s)1.00millilitre(s)
-
Riboflavin0.50milligram(s)1.00millilitre(s)
-
Nicotinamide23.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cat
-
Dog
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
-
Intravenous use
-
Cat
-
Dog
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Cat
-
Dog
-
Horse
-
Meat and offal0day
-
Milk0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA11BA
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Scanvet Poland Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0736
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
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in another language below.
Polish (PDF)
Published on: 4/02/2022
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
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