Aurofac Granular 250 mg/g Premix for medicated feedingstuff for pigs and chickens
Aurofac Granular 250 mg/g Premix for medicated feedingstuff for pigs and chickens
Authorised
- Chlortetracycline hydrochloride
Product identification
Medicine name:
Aurofac Granular 250 mg/g Premix for medicated feedingstuff for pigs and chickens
Aurofac granular 250 mg/g pré-mistura medicamentosa para alimento medicamentoso para suínos e galinhas
Active substance:
- Chlortetracycline hydrochloride
Target species:
-
Chicken
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Chlortetracycline hydrochloride250.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
Oral use
-
Chicken
-
Eggs4day
-
Meat and offal2day
-
-
Pig
-
Meat and offal10day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- Polyethylene bags containing 2 kg
- Polyethylene bags containing 3 kg
- Polyethylene bags containing 4.8 kg
- Polyethylene bags containing 6.4 kg
- Polyethylene bags containing 8 kg
- Polyethylene bags containing 9 kg
- Polyethylene bags containing 12 kg
- Polyethylene bags containing 16 kg
- Polyethylene bags containing 20 kg
- Polyethylene bags containing 25 kg
- Polyethylene bags containing 3 kg. Cardboard cartons containing 8 x 3 kg.
- Polyethylene bags containing 2 kg. Cardboard cartons containing 12 x 2 kg.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Phibro Animal Health (Poland) Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Medolla Manufacturing S.r.l.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 275/01/10DFVPT
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0207/002
Concerned member states:
-
Portugal
-
Slovenia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
Combined File of all Documents
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Portuguese (PDF)
Published on: 10/12/2025