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Hydrocodone Bitartrate and Acetaminophen
Hydrocodone Bitartrate and Acetaminophen - 68084-362-01 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 68084-362 |
| Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 500; 10 mg/1; mg/1 & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 68084-362 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040148 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090923 |
Package Information of Hydrocodone Bitartrate and Acetaminophen
| Package NDC: | 68084-362-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-362-01) > 10 TABLET in 1 BLISTER PACK (68084-362-11) |
NDC Information of Hydrocodone Bitartrate and Acetaminophen
| NDC Code | 68084-362-01 |
| Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-362-01) > 10 TABLET in 1 BLISTER PACK (68084-362-11) |
| Product NDC | 68084-362 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090923 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 500; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
