# POTASSIUM CHLORIDE

NDC: 17856-0048
Generic name: POTASSIUM CHLORIDE ORAL
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20231005

FDA application: ANDA211648

## Active ingredients

- POTASSIUM CHLORIDE: 1.5 g/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0048"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0048
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc55474c-cc51-4f17-8cb3-0f34b3e68a55