FDA NDC Directory · JSON-LD · Markdown

Folic Acid

NDC 72189-199 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA204418
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20210412
Package count1

External sources

Source: openFDA. Public-domain (CC0).