FDA NDC Directory · JSON-LD · Markdown

FOLIC ACID

NDC 11534-165 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefolic acid
Labeler / ManufacturerSUNRISE PHARMACEUTICAL, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204418
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20150804
Package count3

External sources

Source: openFDA. Public-domain (CC0).