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POTASSIUM CHLORIDE

NDC 63304-078 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208864
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPOTASSIUM CHLORIDE (600 mg/1)
Marketing started20200102
Package count1

External sources

Source: openFDA. Public-domain (CC0).