# Celecoxib

NDC: 43063-825
Generic name: Celecoxib
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20150603
Marketing ended: 20270131
FDA application: ANDA204197

## 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:"43063-825"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-825
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52572bfb-43f0-4b55-b1fd-231a05c8b83e