NDC codes

FDA NDC Directory
Product NDC (as listed)23155-966Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0966Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
23155-966-062315509660660 CAPSULE in 1 BOTTLE (23155-966-06)Marketed from Mar 25, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Celecoxib
Generic name (nonproprietary)
celecoxib
Active ingredients
Celecoxib — 400 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211412
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 23155-966_4d1a2742-47c3-9c75-e063-6294a90aca73SPL ID 4d1a2742-47c3-9c75-e063-6294a90aca73SPL set ID 4bc96d0c-b484-3cee-e063-6294a90a9193RxCUI 205322, 205323, 349514, 686379UNII JCX84Q7J1LUPC 0323155965056, 0323155965018, 0323155963069, 0323155964059, 0323155966060, 0323155964011

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N423155096606 followed by a unit qualifier and the quantity

Package 23155-0966-06. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

1. INDICATIONS AND USAGE Celecoxib capsules are indicated Celecoxib capsule is a nonsteroidal anti-inflammatory drug indicated for: Osteoarthritis (OA) (1.1) Rheumatoid Arthritis (RA) (1.2) Juvenile Rheumatoid Arthritis (JRA) in patients 2 years and older (1.3) Ankylosing Spondylitis (AS) (1.4) Acute Pain (AP) (1.5) Primary Dysmenorrhea (PD) (1.6) 1.1 Osteoarthritis (OA) For the management of the signs and symptoms of OA [ see Clinical Studies (14.1) ] 1.2 Rheumatoid Arthritis (RA) For the management of the signs and symptoms of RA [ see Clinical Studies (14.2) ] 1.3 Juvenile Rheumatoid Arthritis (JRA) For the management of the signs and symptoms of JRA in patients 2 years and older [ see Cl…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211412

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 211412
ProductStrengthForm · routeLabelerProduct NDC
CelecoxibCelecoxib 400 mg/1CapsuleOralYiling Pharmaceutical, Inc.69117-0023
CelecoxibCelecoxib 100 mg/1CapsuleOralChartwell RX, LLC62135-021
CelecoxibCelecoxib 200 mg/1CapsuleOralChartwell RX, LLC62135-022
CelecoxibCelecoxib 400 mg/1CapsuleOralChartwell RX, LLC62135-023
CelecoxibCelecoxib 50 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-963
CelecoxibCelecoxib 100 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-964
CelecoxibCelecoxib 200 mg/1CapsuleOralAvet Pharmaceuticals Inc.23155-965
CelecoxibCelecoxib 200 mg/1CapsuleOralYiling Pharmaceutical, Inc.69117-0022
CelecoxibCelecoxib 50 mg/1CapsuleOralYiling Pharmaceutical, Inc.69117-0020
CelecoxibCelecoxib 100 mg/1CapsuleOralYiling Pharmaceutical, Inc.69117-0021

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Celecoxib NDC 23155-966 | Med-Code