Prescription drug · ANDA
Oxaprozin NDC 72189-595
Oxaprozin 600 mg/1 · Tablet, Film coated · Oral · Direct_Rx
NDC codes
FDA NDC Directory| 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_Rx
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075855
- Marketing start
- Listing expires
- 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
N472189059560followed by a unit qualifier and the quantityPackage 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 . 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.
Other NDCs under ANDA 075855
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| 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 |
| Oxaprozin | Oxaprozin 600 mg/1 | Tablet, Film coatedOral | ST MARY'S MEDICAL PARK PHARMACY | 60760-382 |