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Acyclovir

NDC 69117-0018 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerYILING PHARMACEUTICAL, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA210401
Dosage form / routeTABLET · ORAL
Active ingredientsACYCLOVIR (400 mg/1)
Marketing started20180504
Package count2

External sources

Source: openFDA. Public-domain (CC0).