Neomin, 1000 mg/g geriamieji milteliai, skirti naudoti su geriamuoju vandeniu, pašaru, pienu ar pieno pakaitalu galvijams (veršeliams), kiaulėms ir vištoms (jaunoms vištaitėms, dedeklėms ir veislinėms vištoms)
Neomin, 1000 mg/g geriamieji milteliai, skirti naudoti su geriamuoju vandeniu, pašaru, pienu ar pieno pakaitalu galvijams (veršeliams), kiaulėms ir vištoms (jaunoms vištaitėms, dedeklėms ir veislinėms vištoms)
Authorised
- NEOMYCIN SULFATE
Product identification
Medicine name:
Neomin, 1000 mg/g geriamieji milteliai, skirti naudoti su geriamuoju vandeniu, pašaru, pienu ar pieno pakaitalu galvijams (veršeliams), kiaulėms ir vištoms (jaunoms vištaitėms, dedeklėms ir veislinėms vištoms)
Active substance:
- NEOMYCIN SULFATE
Target species:
-
Pig
-
Cattle (calf)
-
Chicken
Route of administration:
-
In drinking water/milk use
-
In-feed use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In drinking water/milk use
- Pig
-
Meat and offal14day
-
- Cattle (calf)
-
Meat and offal14day
-
- Chicken
-
Meat and offal7day
-
Egg0day
-
-
In-feed use
- Pig
-
Meat and offal14day
-
- Chicken
-
Meat and offal7day
-
Egg0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
- Bela-Pharm GmbH & Co. KG
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/07/1737/001-006
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV1737.pdf
Lithuanian (PDF)
Download Published on: 3/08/2022
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