FDA NDC Directory · JSON-LD · Markdown

Potassium Chloride

NDC 17856-1458 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA210041
Dosage form / routeSOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (3 g/15mL)
Marketing started20180724
Package count1

External sources

Source: openFDA. Public-domain (CC0).