FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 60687-855 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA211667
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1.5 g/1.58g)
Marketing started20250328
Package count2

External sources

Source: openFDA. Public-domain (CC0).