FDA NDC Directory · JSON-LD · Markdown

Potassium Citrate

NDC 0245-0070 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepotassium citrate
Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryNew Drug Application (innovator) · App NDA019071
Dosage form / routeTABLET · ORAL
Active ingredientsPOTASSIUM CITRATE (5 meq/1)
Marketing started20060901
Marketing ended20270731
Package count1

External sources

Source: openFDA. Public-domain (CC0).