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Acyclovir

NDC 63323-325 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameacyclovir
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074930
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsACYCLOVIR SODIUM (50 mg/mL)
Marketing started20001017
Package count2

External sources

Source: openFDA. Public-domain (CC0).