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
- 76420-842_327a5fba-3c08-7bba-e063-6294a90a75e5
- Product NDC
- 76420-842
- Form
- CAPSULE
- Composition / generic term
- Celecoxib
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201203
- Source listing expiry
- 20261231
Source-listed ingredients
- CELECOXIB — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE in 1 BOTTLE (76420-842-00) · 76420-842-00
- 1 CAPSULE in 1 BOTTLE (76420-842-01) · 76420-842-01
- 7 CAPSULE in 1 BOTTLE (76420-842-07) · 76420-842-07
- 14 CAPSULE in 1 BOTTLE (76420-842-14) · 76420-842-14
- 20 CAPSULE in 1 BOTTLE (76420-842-20) · 76420-842-20
- 30 CAPSULE in 1 BOTTLE (76420-842-30) · 76420-842-30
- 60 CAPSULE in 1 BOTTLE (76420-842-60) · 76420-842-60
- 90 CAPSULE in 1 BOTTLE (76420-842-90) · 76420-842-90
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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