FDA NDC Directory · JSON-LD · Markdown

Lithium

NDC 0121-1027 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA070755
Dosage form / routeSOLUTION · ORAL
Active ingredientsLITHIUM CITRATE (8 meq/5mL)
Marketing started20260414
Package count1

External sources

Source: openFDA. Public-domain (CC0).