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
42806-722_2b20721c-b138-1932-e063-6394a90ae66e
Product NDC
42806-722
Form
CAPSULE
Composition / generic term
Celecoxib
Labeler
EPIC PHARMA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20201016
Source listing expiry
20261231

Source-listed ingredients

  • CELECOXIB — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (42806-722-01) · 42806-722-01
  • 500 CAPSULE in 1 BOTTLE (42806-722-05) · 42806-722-05

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.

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