# Potassium Chloride Extended-Release

NDC: 63304-076
Generic name: Potassium Chloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191120

FDA application: ANDA076368

## Active ingredients

- POTASSIUM CHLORIDE: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-076"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-076
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ed8ea55-8b15-f718-e053-2a95a90a587a