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Oxaprozin
Oxaprozin - 0185-0141-01 - (Oxaprozin)
Drug Information of Oxaprozin
| Product NDC: | 0185-0141 |
| Proprietary Name: | Oxaprozin |
| Non Proprietary Name: | Oxaprozin |
| Active Ingredient(s): | 600 mg/1 & nbsp; Oxaprozin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxaprozin
| Product NDC: | 0185-0141 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075845 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010131 |
Package Information of Oxaprozin
| Package NDC: | 0185-0141-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0185-0141-01) |
NDC Information of Oxaprozin
| NDC Code | 0185-0141-01 |
| Proprietary Name | Oxaprozin |
| Package Description | 100 TABLET in 1 BOTTLE (0185-0141-01) |
| Product NDC | 0185-0141 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxaprozin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010131 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| 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] |
