FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 0121-1896 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic namePOTASSIUM CHLORIDE
Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA210766
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (20 meq/30mL)
Marketing started20230327
Package count3

External sources

Source: openFDA. Public-domain (CC0).