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NORCO
NORCO - 63629-2946-5 - (Hydrocodone bitartrate and acetaminophen)
Drug Information of NORCO
| Product NDC: | 63629-2946 |
| Proprietary Name: | NORCO |
| Non Proprietary Name: | Hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 235; 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 NORCO
| Product NDC: | 63629-2946 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040099 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090811 |
Package Information of NORCO
| Package NDC: | 63629-2946-5 |
| Package Description: | 90 TABLET in 1 BOTTLE (63629-2946-5) |
NDC Information of NORCO
| NDC Code | 63629-2946-5 |
| Proprietary Name | NORCO |
| Package Description | 90 TABLET in 1 BOTTLE (63629-2946-5) |
| Product NDC | 63629-2946 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090811 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 235; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
