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Hydrocodone Bitartrate and Acetaminophen
Hydrocodone Bitartrate and Acetaminophen - 62037-567-05 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 62037-567 |
| Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 660; 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: | 62037-567 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040495 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030528 |
Package Information of Hydrocodone Bitartrate and Acetaminophen
| Package NDC: | 62037-567-05 |
| Package Description: | 500 TABLET in 1 BOTTLE, PLASTIC (62037-567-05) |
NDC Information of Hydrocodone Bitartrate and Acetaminophen
| NDC Code | 62037-567-05 |
| Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (62037-567-05) |
| Product NDC | 62037-567 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030528 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 660; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
