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REPREXAIN
REPREXAIN - 23710-900-01 - (Hydrocodone Bitartrate and Ibuprofen)
Drug Information of REPREXAIN
| Product NDC: | 23710-900 |
| Proprietary Name: | REPREXAIN |
| Non Proprietary Name: | Hydrocodone Bitartrate and Ibuprofen |
| Active Ingredient(s): | 2.5; 200 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate and Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REPREXAIN
| Product NDC: | 23710-900 |
| Labeler Name: | Quinnova Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076642 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100218 |
Package Information of REPREXAIN
| Package NDC: | 23710-900-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (23710-900-01) |
NDC Information of REPREXAIN
| NDC Code | 23710-900-01 |
| Proprietary Name | REPREXAIN |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (23710-900-01) |
| Product NDC | 23710-900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100218 |
| Marketing Category Name | ANDA |
| Labeler Name | Quinnova Pharmaceuticals, LLC |
| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
| Strength Number | 2.5; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC],Opioid Agonist [EPC],Opioid Agonists [MoA] |
