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Potassium Chloride

NDC 69238-1458 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210041
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (3 g/15mL)
Marketing started20180724
Package count2

External sources

Source: openFDA. Public-domain (CC0).