# Diclofenac Sodium Delayed Release

NDC: 61442-103
Generic name: Diclofenac Sodium
Labeler / Manufacturer: Carlsbad Technology, Inc.
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61442-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61442-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40879600-ba6c-43a8-aa5d-d0d41503d593