FDA NDC Directory · JSON-LD · Markdown

LITHOBID

NDC 62559-280 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namelithium carbonate
Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018027
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsLITHIUM CARBONATE (300 mg/1)
Marketing started20140701
Package count1

External sources

Source: openFDA. Public-domain (CC0).