| Product NDC: | 12634-264 |
| Proprietary Name: | Hydrocodone Bitartrate with Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitartrate with Acetaminophen |
| Active Ingredient(s): | 325; 5 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate with Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 12634-264 |
| Labeler Name: | Apotheca Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040099 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090312 |
| Package NDC: | 12634-264-57 |
| Package Description: | 20 TABLET in 1 BLISTER PACK (12634-264-57) |
| NDC Code | 12634-264-57 |
| Proprietary Name | Hydrocodone Bitartrate with Acetaminophen |
| Package Description | 20 TABLET in 1 BLISTER PACK (12634-264-57) |
| Product NDC | 12634-264 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate with Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090312 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotheca Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 325; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |