FDA NDC Directory · JSON-LD · Markdown

POTASSIUM CHLORIDE

NDC 71656-022 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSaptalis Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211648
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (3 g/15mL)
Marketing started20231005
Package count3

External sources

Source: openFDA. Public-domain (CC0).