Nalgosed, 10mg/ml, Solution for injection
  • BUTORPHANOL
  • Valid
Authorised in these countries:
  • Slovakia
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Product identification

Medicine name:
Nalgosed, 10mg/ml, Solution for injection
NALGOSED 10 mg/ml injekčný roztok
Active substance and strength:
  • BUTORPHANOL
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QN02AF01
Authorisation number:
  • 96/035/MR/19-S
Product identification number:
  • 60781e20-0f85-4875-816f-f3db99f1597e
Permanent identification number:
  • 600000054505

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
    • Cat
    • Dog
  • Intravenous use
    • Horse
      • Meat
        0
        day
      • Milk
        0
        day
    • Cat
    • Dog
  • Subcutaneous use
    • Cat
    • Dog

Availability

Package description:
  • Glass Vial
Manufacturing sites for batch release:
  • Bioveta a.s.
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:
  • CZ/V/0142/001
Date of authorisation status change:
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
  • Slovakia
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Marketing authorisation holder:
  • Bioveta a.s.
Marketing authorisation issued:
Reference member state:
  • Czechia
Concerned member states:
  • Bulgaria
  • Estonia
  • Greece
  • Hungary
  • Latvia
  • Lithuania
  • Poland
  • Romania
  • Slovakia
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

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