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
- 76420-009_045987eb-8735-65e2-e063-6394a90a9699
- Product NDC
- 76420-009
- Form
- CAPSULE
- Composition / generic term
- celecoxib
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160316
- Source listing expiry
- 20261231
Source-listed ingredients
- CELECOXIB — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CAPSULE in 1 BOTTLE (76420-009-01) · 76420-009-01
- 7 CAPSULE in 1 BOTTLE (76420-009-07) · 76420-009-07
- 14 CAPSULE in 1 BOTTLE (76420-009-14) · 76420-009-14
- 20 CAPSULE in 1 BOTTLE (76420-009-20) · 76420-009-20
- 30 CAPSULE in 1 BOTTLE (76420-009-30) · 76420-009-30
- 60 CAPSULE in 1 BOTTLE (76420-009-60) · 76420-009-60
- 90 CAPSULE in 1 BOTTLE (76420-009-90) · 76420-009-90
Source and coverage
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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.
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