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
16714-734_967b9589-e174-4600-988e-d11eea0845ab
Product NDC
16714-734
Form
CAPSULE
Composition / generic term
CELECOXIB
Labeler
NorthStar RxLLC
Marketing category
ANDA
Marketing start / end (source format)
20170926
Source listing expiry
20261231

Source-listed ingredients

  • CELECOXIB — 400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 CAPSULE in 1 BOTTLE (16714-734-01) · 16714-734-01

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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