# Diclofenac Potassium

NDC: 71335-2052
Generic name: diclofenac potassium
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20201219

FDA application: ANDA075229

## Active ingredients

- DICLOFENAC POTASSIUM: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86461915-9bc1-43d4-8d92-6eef3e56bd90