# Diclofenac Sodium

NDC: 60687-606
Generic name: Diclofenac Sodium
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20220607

FDA application: ANDA090066

## 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:"60687-606"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-606
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63c00b50-06d3-4659-81cf-be4516429e81