United States · FDA National Drug Code directory
Celecoxib
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50228-159_8143c6b3-7c13-4abe-af2a-23fbe3e6d48a
- Product NDC
- 50228-159
- Form
- CAPSULE
- Composition / generic term
- Celecoxib
- Labeler
- ScieGen Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201203
- Source listing expiry
- 20271231
Source-listed ingredients
- CELECOXIB — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE in 1 BOTTLE (50228-159-05) · 50228-159-05
- 30 CAPSULE in 1 BOTTLE (50228-159-30) · 50228-159-30
- 60 CAPSULE in 1 BOTTLE (50228-159-60) · 50228-159-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →