FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 62037-559 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077419
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started20080825
Marketing ended20260630
Package count2

External sources

Source: openFDA. Public-domain (CC0).