# Celecoxib

NDC: 80425-0040
Generic name: Celecoxib
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20180601

FDA application: ANDA204776

## Active ingredients

- CELECOXIB: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0040"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0040
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af9da1f2-717b-32b6-e053-2995a90ae585
