FDA NDC Directory · JSON-LD · Markdown

Acyclovir

NDC 71921-146 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075090
Dosage form / routeCAPSULE · ORAL
Active ingredientsACYCLOVIR (200 mg/1)
Marketing started20260218
Package count1

External sources

Source: openFDA. Public-domain (CC0).