NDC codes

FDA NDC Directory
Product NDC (as listed)72241-023Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72241-0023Add 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
72241-023-037224100230360 CAPSULE in 1 BOTTLE (72241-023-03)Marketed from Aug 23, 2021
72241-023-0572241002305100 CAPSULE in 1 BOTTLE (72241-023-05)Marketed from Aug 23, 2021
72241-023-1072241002310500 CAPSULE in 1 BOTTLE (72241-023-10)Marketed from Aug 23, 2021
72241-023-11722410023111000 CAPSULE in 1 BOTTLE (72241-023-11)Marketed from Aug 23, 2021

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 — 100 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208701
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 72241-023_75f7a2cd-9aa3-4f66-a708-f3f6a8a571daSPL ID 75f7a2cd-9aa3-4f66-a708-f3f6a8a571daSPL set ID b0f73074-f3d8-4812-8e64-f88a02869ed3RxCUI 205322, 205323, 349514, 686379UNII JCX84Q7J1L

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

N472241002303 followed by a unit qualifier and the quantity

Package 72241-0023-03. 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)

Celecoxib capsules are indicated Celecoxib capsules are a non-steroidal 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 [s…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208701

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

FDA NDC Directory listings under ANDA 208701
ProductStrengthForm · routeLabelerProduct NDC
CelecoxibCelecoxib 200 mg/1CapsuleOralBryant Ranch Prepack72162-2421
CelecoxibCelecoxib 100 mg/1CapsuleOralREMEDYREPACK INC.70518-4009
CelecoxibCelecoxib 200 mg/1CapsuleOralModavar Pharmaceuticals LLC72241-024
CelecoxibCelecoxib 50 mg/1CapsuleOralModavar Pharmaceuticals LLC72241-022
CelecoxibCelecoxib 400 mg/1CapsuleOralModavar Pharmaceuticals LLC72241-025
CelecoxibCelecoxib 200 mg/1CapsuleOralCadila Pharmaceuticals Limited71209-056
CelecoxibCelecoxib 50 mg/1CapsuleOralCadila Pharmaceuticals Limited71209-054
CelecoxibCelecoxib 100 mg/1CapsuleOralCadila Pharmaceuticals Limited71209-055
CelecoxibCelecoxib 400 mg/1CapsuleOralCadila Pharmaceuticals Limited71209-057

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