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Potassium Citrate

NDC 63629-8759 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA209758
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CITRATE (10 meq/1)
Marketing started20180530
Package count1

External sources

Source: openFDA. Public-domain (CC0).