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Potassium Chloride for Oral Solution

NDC 10135-807 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerMarlex Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212183
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsPOTASSIUM CHLORIDE (1.5 g/1.58g)
Marketing started20250801
Package count2

External sources

Source: openFDA. Public-domain (CC0).