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Folic Acid

NDC 71209-007 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCadila Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202437
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20181120
Package count2

External sources

Source: openFDA. Public-domain (CC0).