FDA NDC Directory · JSON-LD · Markdown

Lithium Carbonate

NDC 60687-964 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA079139
Dosage form / routeCAPSULE · ORAL
Active ingredientsLITHIUM CARBONATE (600 mg/1)
Marketing started20260614
Package count1

External sources

Source: openFDA. Public-domain (CC0).