FDA NDC Directory · JSON-LD · Markdown

FOLIC ACID

NDC 69315-127 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLeading Pharma, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040796
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20090112
Package count2

External sources

Source: openFDA. Public-domain (CC0).