# up and up arthritis pain reliever

NDC: 11673-569
Generic name: diclofenac sodium
Labeler / Manufacturer: Target Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20200819

FDA application: ANDA211253

## 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:"11673-569"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-569
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0b7ae58c-cdaf-4343-a199-7a90bf901eb5