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oxaprozin
oxaprozin - 59762-6002-1 - (OXAPROZIN)
Drug Information of oxaprozin
| Product NDC: | 59762-6002 |
| Proprietary Name: | oxaprozin |
| Non Proprietary Name: | OXAPROZIN |
| Active Ingredient(s): | 600 mg/1 & nbsp; OXAPROZIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxaprozin
| Product NDC: | 59762-6002 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018841 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130328 |
Package Information of oxaprozin
| Package NDC: | 59762-6002-1 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (59762-6002-1) |
NDC Information of oxaprozin
| NDC Code | 59762-6002-1 |
| Proprietary Name | oxaprozin |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (59762-6002-1) |
| Product NDC | 59762-6002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXAPROZIN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130328 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | OXAPROZIN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
