What is NDC 72189-595?

72189-595 is the product NDC for Oxaprozin, Oxaprozin 600 mg/1 tablet, film coated, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Oxaprozin?

8 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Oxaprozin NDC 72189-595 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-595Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0595Add 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 NDC	11-digit (billing)	Package	Copy
72189-595-60	72189059560	60 TABLET, FILM COATED in 1 BOTTLE (72189-595-60)Marketed from Dec 2, 2024

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): Oxaprozin
Generic name (nonproprietary): oxaprozin
Active ingredients: Oxaprozin — 600 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075855
Marketing start: Dec 2, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers: Product ID 72189-595_284ce161-0a4b-8999-e063-6394a90aa60aSPL ID 284ce161-0a4b-8999-e063-6394a90aa60aSPL set ID 284ce161-0a4a-8999-e063-6394a90aa60aRxCUI 312132UNII MHJ80W9LRB
Pharmacologic class: Nonsteroidal Anti-inflammatory Drug

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

N472189059560 followed by a unit qualifier and the quantity

Package 72189-0595-60. 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 Dec 2, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Oxaprozin tablets are indicated: For relief of the signs and symptoms of osteoarthritis For relief of the signs and symptoms of rheumatoid arthritis For relief of the signs and symptoms of juvenile rheumatoid arthritis

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-595

What is NDC 72189-595?: 72189-595 is the product NDC for Oxaprozin, Oxaprozin 600 mg/1 tablet, film coated, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Oxaprozin.
What is the active ingredient?: Oxaprozin.
Who is the labeler?: Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxaprozin?: 8 other product NDCs are listed under this name. See all Oxaprozin NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Oxaprozin NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Oxaprozin	Oxaprozin 300 mg/1	CapsuleOral	SOLA Pharmaceuticals, LLC	70512-787	70512-0787-60
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	ST MARY'S MEDICAL PARK PHARMACY	60760-382	60760-0382-14
Oxaprozin	Oxaprozin 600 mg/1	TabletOral	Amneal Pharmaceuticals NY LLC	69238-1120	69238-1120-0169238-1120-05
Oxaprozin	Oxaprozin 600 mg/1	TabletOral	Bryant Ranch Prepack	71335-0617	71335-0617-0171335-0617-0271335-0617-03+4 more
Oxaprozin	Oxaprozin 600 mg/1	TabletOral	Chartwell RX, LLC.	62135-176	62135-0176-1862135-0176-60
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0393	71335-0393-0171335-0393-0271335-0393-03+4 more
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Limited	55111-170	55111-0170-0155111-0170-05
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-261	82804-0261-60

Other NDCs under ANDA 075855

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

FDA NDC Directory listings under ANDA 075855
Product	Strength	Form · route	Labeler	Product NDC
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	ST MARY'S MEDICAL PARK PHARMACY	60760-382
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0393
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Limited	55111-170
Oxaprozin	Oxaprozin 600 mg/1	Tablet, Film coatedOral	Proficient Rx LP	82804-261