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Potassium Chloride

NDC 53041-420 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerGuardian Drug Company
Marketing categoryAbbreviated NDA (generic) · App ANDA219009
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1.5 g/1.57g)
Marketing started20250722
Package count2

External sources

Source: openFDA. Public-domain (CC0).