FDA NDC Directory · JSON-LD · Markdown

Celecoxib

NDC 0904-6503 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA204197
Dosage form / routeCAPSULE · ORAL
Active ingredientsCELECOXIB (200 mg/1)
Marketing started20150625
Marketing ended20260630
Package count1

External sources

Source: openFDA. Public-domain (CC0).