Sulphix
Sulphix
Authorised
- Trimethoprim
- Sulfadoxine
Product identification
Medicine name:
Sulphix
Active substance:
- Trimethoprim
- Sulfadoxine
Target species:
-
Cattle
-
Goat
-
Horse
-
Pig
-
Cat
-
Guinea pig
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Trimethoprim40.00/milligram(s)1.00millilitre(s)
-
Sulfadoxine200.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Milk4day
-
Meat and offal4day
-
-
Goat
-
Milk4day
-
Meat and offal4day
-
-
Horse
-
Meat and offal4day
-
Milkno withdrawal periodNicht bei Stuten anwenden, deren Milch fur den menschlichen Verzehr vorgesehen ist.
-
-
Pig
-
Meat and offal5day
-
-
-
Intramuscular use
-
Cattle
-
Milk4day
-
Meat and offal11day
-
-
Goat
-
Meat and offal11day
-
Milk4day
-
-
Pig
-
Meat and offal14day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
- Available only in German
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 6856907.00.00
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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in another language below.
German (PDF)
Published on: 29/07/2025