FDA NDC Directory · JSON-LD · Markdown

Celecoxib

NDC 43063-825 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204197
Dosage form / routeCAPSULE · ORAL
Active ingredientsCELECOXIB (200 mg/1)
Marketing started20150603
Marketing ended20270131
Package count4

External sources

Source: openFDA. Public-domain (CC0).