# Diclofenac Sodium

NDC: 68788-8784
Generic name: Diclofenac Sodium
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20241212

FDA application: ANDA090066

## Active ingredients

- DICLOFENAC SODIUM: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4ee64a93-9965-47c8-be2c-14232df44b2b