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NDC 59762-6002-01 oxaprozin 600 mg/1 Details
oxaprozin 600 mg/1
oxaprozin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Greenstone LLC. The primary component is OXAPROZIN.
MedlinePlus Drug Summary
Oxaprozin is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Oxaprozin is also used to relieve pain, tenderness, swelling, and stiffness caused by juvenile rheumatoid arthritis in children 6 years of age and older. Oxaprozin is in a class of medications called nonsteroidal anti-inflammatory medications (NSAIDs). It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
Related Packages: 59762-6002-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Oxaprozin
Product Information
| NDC | 59762-6002 |
|---|---|
| Product ID | 59762-6002_fcadb9d0-958e-4d05-97a7-5b18dbf6e230 |
| Associated GPIs | 66100065000320 |
| GCN Sequence Number | 017204 |
| GCN Sequence Number Description | oxaprozin TABLET 600 MG ORAL |
| HIC3 | S2B |
| HIC3 Description | NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS |
| GCN | 01750 |
| HICL Sequence Number | 006620 |
| HICL Sequence Number Description | OXAPROZIN |
| Brand/Generic | Generic |
| Proprietary Name | oxaprozin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | oxaprozin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 600 |
| Active Ingredient Units | mg/1 |
| Substance Name | OXAPROZIN |
| Labeler Name | Greenstone LLC |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA AUTHORIZED GENERIC |
| Application Number | NDA018841 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 59762-6002-01 (59762600201)
| NDC Package Code | 59762-6002-1 |
|---|---|
| Billing NDC | 59762600201 |
| Package | 100 TABLET, FILM COATED in 1 BOTTLE (59762-6002-1) |
| Marketing Start Date | 2013-03-27 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.60587 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | OXAPROZIN 600 MG CAPLET |
| Pharmacy Type Indicator | C/I |
| OTC | N |
| Explanation Code | 1, 6 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |