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Potassium Chloride

NDC 68462-357 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA202868
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20160120
Package count3

External sources

Source: openFDA. Public-domain (CC0).