FDA NDC Directory · JSON-LD · Markdown

Folic Acid

NDC 58657-151 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMethod Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211064
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20180209
Package count2

External sources

Source: openFDA. Public-domain (CC0).