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Lithium Carbonate

NDC 43063-901 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076691
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsLITHIUM CARBONATE (450 mg/1)
Marketing started20040113
Package count2

External sources

Source: openFDA. Public-domain (CC0).