FDA NDC Directory · JSON-LD · Markdown

Folic Acid

NDC 70518-4338 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA202437
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20250513
Package count1

External sources

Source: openFDA. Public-domain (CC0).