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Lithium Carbonate

NDC 46708-305 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA079159
Dosage form / routeCAPSULE · ORAL
Active ingredientsLITHIUM CARBONATE (600 mg/1)
Marketing started20161227
Package count3

External sources

Source: openFDA. Public-domain (CC0).