SG.PENI.4T

PRODUCT INFORMATION
Livestock Antibiotic Injection

SG.PENI.4T

Antibiotic powder for injection containing Penicillin G sodium and Penicillin G procain, used in cattle, buffaloes, calves, buffalo calves and pigs for the treatment of arthritis, hoof inflammation, swine erysipelas and pasteurellosis according to the instructions on the product label.

KEY INGREDIENTS
Penicillin G sodium; Penicillin G procain.
DOSAGE FORM / ROUTE OF USE
Powder for injection. Reconstitute with water for injection and administer intramuscularly.
MAIN USES
Treatment of arthritis, hoof inflammation, swine erysipelas and pasteurellosis.
TARGET SPECIES
Cattle, buffaloes, calves, buffalo calves and pigs.
View details
Use according to the instructions on the product label.
DETAILED INFORMATION
SG.PENI.4T – Powder for injection
Main group: Livestock Product group: Antibiotic Route of use: Injection

1. COMPOSITION / QUALITY SPECIFICATIONS

Composition:

  • Penicillin G sodium.
  • Penicillin G procain.

The old website does not specify the concentration of each active ingredient. The official label, catalogue or packshot should be checked if the CMS requires the concentrations to be displayed.

2. INDICATIONS

Treatment of arthritis, hoof inflammation, swine erysipelas and pasteurellosis in cattle, buffaloes, calves, buffalo calves and pigs.

3. ADMINISTRATION & DOSAGE

Reconstitute the product with 20 ml water for injection. Administer intramuscularly 1 - 2 times daily for 4 - 5 consecutive days.

Cattle, buffaloes
1 vial / 200 kg body weight.
Adult pigs, calves, buffalo calves
1 vial / 100 - 150 kg body weight.
Piglets
1 vial / 60 - 80 kg body weight.

4. DOSAGE FORM / ROUTE OF USE

  • Powder for injection.
  • Reconstitute with water for injection before use.
  • Route of administration: intramuscular injection.

5. PRECAUTIONS

  • Use according to the instructions on the product label or as directed by a veterinary professional.
  • Reconstitute with the correct amount of water for injection and shake well before use.
  • Do not alter the dosage, route of administration or treatment duration without professional guidance.
  • The official label, catalogue or packshot should be checked to confirm the active ingredient concentrations and withdrawal period before publishing complete information on the CMS.

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