FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 62037-560 · 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 (750 mg/1)
Marketing started20080825
Marketing ended20261031
Package count4

External sources

Source: openFDA. Public-domain (CC0).