Active Ingredient: ACYCLOVIR SODIUM
Proprietary Name: ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 500MG BASE/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074885
Product Number: 001
Approval Date: Dec 19, 1997
Applicant Holder Full Name: EUROHEALTH INTERNATIONAL SARL
Marketing Status:
Discontinued
Patent and Exclusivity Information