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
- 72189-360_5a0b313a-2ab3-0d47-e063-6394a90ad440
- Product NDC
- 72189-360
- Form
- CAPSULE
- Composition / generic term
- Celecoxib
- Labeler
- DirectRx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220608
- Source listing expiry
- 20271231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CAPSULE in 1 BOTTLE (72189-360-10) · 72189-360-10
- 30 CAPSULE in 1 BOTTLE (72189-360-30) · 72189-360-30
- 42 CAPSULE in 1 BOTTLE (72189-360-42) · 72189-360-42
- 60 CAPSULE in 1 BOTTLE (72189-360-60) · 72189-360-60
- 120 CAPSULE in 1 BOTTLE (72189-360-72) · 72189-360-72
- 90 CAPSULE in 1 BOTTLE (72189-360-90) · 72189-360-90
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 →