Veterinary Medicines

Tetra-Delta Milking Cow

Not authorised
  • NEOMYCIN SULFATE
  • Prednisolone
  • Benzylpenicillin procaine
  • Novobiocin sodium
  • Dihydrostreptomycin sulfate
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Product identification

Medicine name:
Tetra-Delta Milking Cow
Active substance:
  • NEOMYCIN SULFATE
  • Prednisolone
  • Benzylpenicillin procaine
  • Novobiocin sodium
  • Dihydrostreptomycin sulfate
Target species:
  • Cattle
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • NEOMYCIN SULFATE
    121.76
    milligram(s)
    /
    10.00
    millilitre(s)
  • Prednisolone
    10.00
    milligram(s)
    /
    10.00
    millilitre(s)
  • Benzylpenicillin procaine
    100.00
    milligram(s)
    /
    10.00
    millilitre(s)
  • Novobiocin sodium
    103.69
    milligram(s)
    /
    10.00
    millilitre(s)
  • Dihydrostreptomycin sulfate
    116.81
    milligram(s)
    /
    10.00
    millilitre(s)
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle
      • Meat and offal
        7
        day
      • Milk
        108
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51RV01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • 12ml low density polyethylene syringe filled to 10ml with a sterile suspension. Low density polyethylene plunger. Low density polyethylene base cap. Low density polyethylene tip cap. Cardboard box containing 24 x 10ml syringes.

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:
  • Zoetis Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Zoetis Belgium
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10387/078/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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