# Arthritis Pain Reliever

NDC: 68016-171
Generic name: Diclofenac sodium
Labeler / Manufacturer: Chain Drug Consortium, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20221231
Marketing ended: 20261231
FDA application: ANDA208077

## Active ingredients

- DICLOFENAC SODIUM: 10 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68016-171"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-171
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8879a2ed-6c66-4489-8adc-9f160241cc7d