# Diclofenac Potassium

NDC: 70512-750
Generic name: diclofenac potassium
Labeler / Manufacturer: SOLA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20241021

FDA application: ANDA215787

## 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:"70512-750"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-750
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e770efc8-bbad-4103-98e4-e31019a540f5