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POTASSIUM CITRATE

NDC 16571-865 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namepotassium citrate
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077440
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CITRATE (1080 mg/1)
Marketing started20241215
Package count1

External sources

Source: openFDA. Public-domain (CC0).