FDA NDC Directory · JSON-LD · Markdown

CELECOXIB

NDC 60290-018 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerUmedica Laboratories USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210628
Dosage form / routeCAPSULE · ORAL
Active ingredientsCELECOXIB (200 mg/1)
Marketing started20260215
Package count3

External sources

Source: openFDA. Public-domain (CC0).