# Diclofenac Sodium Delayed Release Delayed Release

NDC: 70882-128
Generic name: Diclofenac Sodium
Labeler / Manufacturer: Cambridge Therapeutics Technologies, LLC
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:"70882-128"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70882-128
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd544812-d7a9-47c8-9148-bea26c8b66c7