# Diclofenac Sodium Delayed Release

NDC: 61145-101
Generic name: Diclofenac Sodium
Labeler / Manufacturer: REPHARM LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20170927

FDA application: ANDA075185

## 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:"61145-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61145-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2d71822-a7f3-447c-911c-971a21af5346