FDA NDC Directory · JSON-LD · Markdown

Celecoxib

NDC 60505-3849 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA204197
Dosage form / routeCAPSULE · ORAL
Active ingredientsCELECOXIB (200 mg/1)
Marketing started20150603
Marketing ended20270531
Package count2

External sources

Source: openFDA. Public-domain (CC0).