# CELECOXIB

NDC: 70247-009
Generic name: Celecoxib
Labeler / Manufacturer: Qingdao BAHEAL Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20161010

FDA application: ANDA208856

## Active ingredients

- CELECOXIB: 400 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70247-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70247-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87c16a33-5eb0-40b0-a020-ed924326f697