# Diclofenac Sodium Delayed Release

NDC: 71335-0481
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: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-0481"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-0481
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae0add8e-3a8a-4c5d-af3b-907f64211fef