# Diclofenac Sodium Delayed Release

NDC: 63629-2013
Generic name: Diclofenac Sodium
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 19981113

FDA application: ANDA075185

## Active ingredients

- DICLOFENAC SODIUM: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-2013"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2013
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6a1ff58-a541-46f8-9663-eed53b7cf392