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Acyclovir

NDC 62332-248 · HUMAN PRESCRIPTION DRUG · OINTMENT

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209000
Dosage form / routeOINTMENT · CUTANEOUS
Active ingredientsACYCLOVIR (50 mg/g)
Marketing started20250327
Package count3

External sources

Source: openFDA. Public-domain (CC0).