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Hydrocodone Bitartate and Acetaminophen
Hydrocodone Bitartate and Acetaminophen - 68788-9754-9 - (HYDROCODONE BITARTRATE, ACETAMINOPHEN)
Drug Information of Hydrocodone Bitartate and Acetaminophen
| Product NDC: | 68788-9754 |
| Proprietary Name: | Hydrocodone Bitartate and Acetaminophen |
| Non Proprietary Name: | HYDROCODONE BITARTRATE, ACETAMINOPHEN |
| Active Ingredient(s): | 325; 2.5 mg/1; mg/1 & nbsp; HYDROCODONE BITARTRATE, ACETAMINOPHEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitartate and Acetaminophen
| Product NDC: | 68788-9754 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040846 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120814 |
Package Information of Hydrocodone Bitartate and Acetaminophen
| Package NDC: | 68788-9754-9 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (68788-9754-9) |
NDC Information of Hydrocodone Bitartate and Acetaminophen
| NDC Code | 68788-9754-9 |
| Proprietary Name | Hydrocodone Bitartate and Acetaminophen |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (68788-9754-9) |
| Product NDC | 68788-9754 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCODONE BITARTRATE, ACETAMINOPHEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120814 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 325; 2.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
