FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 69543-451 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerVirtus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210200
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1.5 g/1.77g)
Marketing started20210101
Marketing ended20260831
Package count2

External sources

Source: openFDA. Public-domain (CC0).