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
- 72162-2175_b65f5ec1-7f05-4505-b07d-4dc28a80306b
- Product NDC
- 72162-2175
- Form
- CAPSULE
- Composition / generic term
- Celecoxib
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201203
- Source listing expiry
- 20261231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (72162-2175-3) · 72162-2175-3
- 500 CAPSULE in 1 BOTTLE (72162-2175-5) · 72162-2175-5
- 60 CAPSULE in 1 BOTTLE (72162-2175-6) · 72162-2175-6
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 →