FDA NDC Directory · JSON-LD · Markdown

Lithium

NDC 71656-072 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSaptalis Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217183
Dosage form / routeSOLUTION · ORAL
Active ingredientsLITHIUM CITRATE (8 meq/5mL)
Marketing started20240328
Package count2

External sources

Source: openFDA. Public-domain (CC0).