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
- 85534-0065_562805ed-2a9f-f1c8-e063-6294a90a50ff
- Product NDC
- 85534-0065
- Form
- CAPSULE
- Composition / generic term
- celecoxib
- Labeler
- HAWAII REPACK, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160316
- Source listing expiry
- 20271231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE (85534-0065-0) · 85534-0065-0
- 60 CAPSULE in 1 BOTTLE (85534-0065-1) · 85534-0065-1
- 90 CAPSULE in 1 BOTTLE (85534-0065-2) · 85534-0065-2
- 120 CAPSULE in 1 BOTTLE (85534-0065-3) · 85534-0065-3
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 →