# POTASSIUM CHLORIDE

NDC: 43598-160
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: Dr. Reddys Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20220725

FDA application: ANDA213062

## Active ingredients

- POTASSIUM CHLORIDE: 40 meq/30mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-160"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-160
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dda82a38-0c08-4947-99b7-915c2949bf16