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Ketoprofen
Ketoprofen - 67296-0369-2 - (Ketoprofen)
Drug Information of Ketoprofen
| Product NDC: | 67296-0369 |
| Proprietary Name: | Ketoprofen |
| Non Proprietary Name: | Ketoprofen |
| Active Ingredient(s): | 75 mg/1 & nbsp; Ketoprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketoprofen
| Product NDC: | 67296-0369 |
| Labeler Name: | RedPharm Drug Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073517 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110118 |
Package Information of Ketoprofen
| Package NDC: | 67296-0369-2 |
| Package Description: | 30 TABLET in 1 BOTTLE (67296-0369-2) |
NDC Information of Ketoprofen
| NDC Code | 67296-0369-2 |
| Proprietary Name | Ketoprofen |
| Package Description | 30 TABLET in 1 BOTTLE (67296-0369-2) |
| Product NDC | 67296-0369 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketoprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110118 |
| Marketing Category Name | ANDA |
| Labeler Name | RedPharm Drug Inc. |
| Substance Name | KETOPROFEN |
| Strength Number | 75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
