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
68071-2733_1ef4a5a5-c001-75ac-e063-6394a90a114a
Product NDC
68071-2733
Form
CAPSULE
Composition / generic term
Celecoxib
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20201203
Source listing expiry
20261231

Source-listed ingredients

  • CELECOXIB — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 40 CAPSULE in 1 BOTTLE (68071-2733-0) · 68071-2733-0
  • 30 CAPSULE in 1 BOTTLE (68071-2733-3) · 68071-2733-3
  • 60 CAPSULE in 1 BOTTLE (68071-2733-6) · 68071-2733-6

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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Celecoxib — United States | Molindra Medicines