LABIDROSOL B SOLUCION INYECTABLE
  • CLORIDRATO DE PIRIDOXINA
  • Dekspantenols
  • Cyanocobalamin
  • Riboflavīna nātrija fosfāts
  • Nicotinamide
  • Thiamine hydrochloride
  • Valid
Authorised in these countries:
  • Spain
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Product identification

Medicine name:
LABIDROSOL B SOLUCION INYECTABLE
Active substance and strength:
  • CLORIDRATO DE PIRIDOXINA
  • Dekspantenols
  • Cyanocobalamin
  • Riboflavīna nātrija fosfāts
  • Nicotinamide
  • Thiamine hydrochloride
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11EA
Authorisation number:
  • 3717 ESP
Product identification number:
  • f3fa2fe3-47bf-4881-948f-0a8fd3678c3f
Permanent identification number:
  • 600000055931

Product details

Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day

Availability

Package description:
Manufacturing sites for batch release:
  • Labiana Life Sciences S.A.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • 3717 ESP
Date of authorisation status change:
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Authorisation country:
  • Spain
Responsible authority:
  • (AEMPS)
Marketing authorisation holder:
  • Labiana
Marketing authorisation issued:
Reference member state:
This information is not available for this product.
Concerned member states:
This information is not available for this product.
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics (PDF)
First published:
Last updated:
Package Leaflet (PDF)
First published:
Last updated:
Labelling (PDF)
First published:
Last updated:
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