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acyclovir

NDC 70518-3436 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204313
Dosage form / routeCAPSULE · ORAL
Active ingredientsACYCLOVIR (200 mg/1)
Marketing started20220614
Package count2

External sources

Source: openFDA. Public-domain (CC0).