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Folic Acid

NDC 0615-8589 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA091145
Dosage form / routeTABLET · ORAL
Active ingredientsFOLIC ACID (1 mg/1)
Marketing started20230710
Package count3

External sources

Source: openFDA. Public-domain (CC0).