# Diclofenac Potassium

NDC: 55700-989
Generic name: diclofenac potassium
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20221122
Marketing ended: 20260630
FDA application: ANDA075229

## Active ingredients

- DICLOFENAC POTASSIUM: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-989"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-989
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da98a208-e2b0-429e-b405-fa7ecca65dc6