Veterinary Medicines

BLAP HELP

Authorised
  • Magnesium acetate
  • Acetylmethionine
  • Glucose
  • L-ARGININE
  • Inositol
  • Calcium gluconate
  • Cyanocobalamin
  • Lysine
  • Thiamine hydrochloride
  • SORBITOL (E420)
  • Nicotinamide
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Product identification

Medicine name:
BLAP HELP
Active substance:
  • Magnesium acetate
  • Acetylmethionine
  • Glucose
  • L-ARGININE
  • Inositol
  • Calcium gluconate
  • Cyanocobalamin
  • Lysine
  • Thiamine hydrochloride
  • SORBITOL (E420)
  • Nicotinamide
Target species:
  • Cattle
Route of administration:
  • Intraperitoneal use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Magnesium acetate
    0.30
    gram(s)
    /
    500.00
    millilitre(s)
  • Acetylmethionine
    12.50
    gram(s)
    /
    500.00
    millilitre(s)
  • Glucose
    10.00
    gram(s)
    /
    500.00
    millilitre(s)
  • L-ARGININE
    0.60
    gram(s)
    /
    500.00
    millilitre(s)
  • Inositol
    5.00
    gram(s)
    /
    500.00
    millilitre(s)
  • Calcium gluconate
    10.00
    gram(s)
    /
    500.00
    millilitre(s)
  • Cyanocobalamin
    0.50
    milligram(s)
    /
    500.00
    millilitre(s)
  • Lysine
    0.60
    gram(s)
    /
    500.00
    millilitre(s)
  • Thiamine hydrochloride
    0.50
    gram(s)
    /
    500.00
    millilitre(s)
  • SORBITOL (E420)
    50.00
    gram(s)
    /
    500.00
    millilitre(s)
  • Nicotinamide
    2.50
    gram(s)
    /
    500.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intraperitoneal use
    • Cattle
      • Milk
        0
        day
  • Intravenous use
    • Cattle
      • Milk
        0
        day
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QV06DE
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Izo S.r.l.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 23/02/2024
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