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
- 71335-2220_4c2347db-b9e2-4521-b094-35fc2e1d4070
- Product NDC
- 71335-2220
- 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
- 15 CAPSULE in 1 BOTTLE (71335-2220-0) · 71335-2220-0
- 30 CAPSULE in 1 BOTTLE (71335-2220-1) · 71335-2220-1
- 60 CAPSULE in 1 BOTTLE (71335-2220-2) · 71335-2220-2
- 90 CAPSULE in 1 BOTTLE (71335-2220-3) · 71335-2220-3
- 14 CAPSULE in 1 BOTTLE (71335-2220-4) · 71335-2220-4
- 20 CAPSULE in 1 BOTTLE (71335-2220-5) · 71335-2220-5
- 10 CAPSULE in 1 BOTTLE (71335-2220-6) · 71335-2220-6
- 180 CAPSULE in 1 BOTTLE (71335-2220-7) · 71335-2220-7
- 28 CAPSULE in 1 BOTTLE (71335-2220-8) · 71335-2220-8
- 56 CAPSULE in 1 BOTTLE (71335-2220-9) · 71335-2220-9
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 →