# Diclofenac Potassium

NDC: 70710-1832
Generic name: Diclofenac Potassium Tablets
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220512

FDA application: ANDA215750

## Active ingredients

- DICLOFENAC POTASSIUM: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1832"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1832
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1aa3d8d6-dd1c-46c7-96f9-2b5c9d72764a