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hydrocodone bitartrate and acetaminophen
hydrocodone bitartrate and acetaminophen - 63629-2958-1 - (hydrocodone bitartrate and acetaminophen)
Drug Information of hydrocodone bitartrate and acetaminophen
| Product NDC: | 63629-2958 |
| Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Non Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 7.5; 200 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: | 63629-2958 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076642 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090930 |
Package Information of hydrocodone bitartrate and acetaminophen
| Package NDC: | 63629-2958-1 |
| Package Description: | 20 TABLET in 1 BOTTLE (63629-2958-1) |
NDC Information of hydrocodone bitartrate and acetaminophen
| NDC Code | 63629-2958-1 |
| Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Package Description | 20 TABLET in 1 BOTTLE (63629-2958-1) |
| Product NDC | 63629-2958 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090930 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | HYDROCODONE BITARTRATE; IBUPROFEN |
| Strength Number | 7.5; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
