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Hydrocodone Bitartrate And Acetaminophen
Hydrocodone Bitartrate And Acetaminophen - 63874-230-30 - (Hydrocodone Bitartrate And Acetaminophen)
Drug Information of Hydrocodone Bitartrate And Acetaminophen
| Product NDC: | 63874-230 |
| 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: | 63874-230 |
| Labeler Name: | Altura Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040157 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of Hydrocodone Bitartrate And Acetaminophen
| Package NDC: | 63874-230-30 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (63874-230-30) |
NDC Information of Hydrocodone Bitartrate And Acetaminophen
| NDC Code | 63874-230-30 |
| Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (63874-230-30) |
| Product NDC | 63874-230 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | Altura Pharmaceuticals, 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] |
