FDA NDC Directory · JSON-LD · Markdown

Celecoxib

NDC 80425-0039 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207446
Dosage form / routeCAPSULE · ORAL
Active ingredientsCELECOXIB (200 mg/1)
Marketing started20170926
Package count2

External sources

Source: openFDA. Public-domain (CC0).