FDA NDC Directory · JSON-LD · Markdown

POTASSIUM CHLORIDE

NDC 60687-653 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA208864
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (750 mg/1)
Marketing started20221020
Package count2

External sources

Source: openFDA. Public-domain (CC0).