NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8571Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8571Add 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
0615-8571-390061585713930 CAPSULE in 1 BLISTER PACK (0615-8571-39)Marketed from Jan 16, 2025

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 200 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206827
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 0615-8571_96cd538d-9ca7-4c69-8054-c27c3ed39262SPL ID 96cd538d-9ca7-4c69-8054-c27c3ed39262SPL set ID 34bef49c-eca1-4f17-9b1b-55900ac40829RxCUI 205322, 205323UNII 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

N400615857139 followed by a unit qualifier and the quantity

Package 00615-8571-39. 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 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 Clinical…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 206827

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

FDA NDC Directory listings under ANDA 206827
ProductStrengthForm · routeLabelerProduct NDC
CelecoxibCelecoxib 200 mg/1CapsuleOralREMEDYREPACK INC.70518-4726
CelecoxibCelecoxib 100 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8572
CelecoxibCelecoxib 200 mg/1CapsuleOralAurobindo Pharma Limited65862-909
CelecoxibCelecoxib 50 mg/1CapsuleOralAurobindo Pharma Limited65862-907
CelecoxibCelecoxib 100 mg/1CapsuleOralAurobindo Pharma Limited65862-908
CelecoxibCelecoxib 400 mg/1CapsuleOralAurobindo Pharma Limited65862-910

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