Home
>
National Drug Code (NDC)
>
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
HYDROCODONE BITARTRATE AND ACETAMINOPHEN - 67296-0642-1 - (hydrocodone bitartrate and acetaminophen)
Drug Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN
| Product NDC: | 67296-0642 |
| Proprietary Name: | HYDROCODONE BITARTRATE AND ACETAMINOPHEN |
| Non Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 750; 7.5 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: | 67296-0642 |
| Labeler Name: | RedPharm Drug Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040157 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960412 |
Package Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN
| Package NDC: | 67296-0642-1 |
| Package Description: | 15 TABLET in 1 BOTTLE (67296-0642-1) |
NDC Information of HYDROCODONE BITARTRATE AND ACETAMINOPHEN
| NDC Code | 67296-0642-1 |
| Proprietary Name | HYDROCODONE BITARTRATE AND ACETAMINOPHEN |
| Package Description | 15 TABLET in 1 BOTTLE (67296-0642-1) |
| Product NDC | 67296-0642 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960412 |
| Marketing Category Name | ANDA |
| Labeler Name | RedPharm Drug Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 750; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
