FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride ER

NDC 72189-462 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA203562
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1500 mg/1)
Marketing started20230417
Package count1

External sources

Source: openFDA. Public-domain (CC0).