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
- 51655-437_4b43d8e7-a5d3-238d-e063-6294a90a33dc
- Product NDC
- 51655-437
- Form
- CAPSULE
- Composition / generic term
- Celecoxib
- Labeler
- Northwind Health Company, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200928
- Source listing expiry
- 20271231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE in 1 BOTTLE, PLASTIC (51655-437-25) · 51655-437-25
- 90 CAPSULE in 1 BOTTLE, PLASTIC (51655-437-26) · 51655-437-26
- 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-437-52) · 51655-437-52
- 14 CAPSULE in 1 BOTTLE, PLASTIC (51655-437-84) · 51655-437-84
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 →