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Hydrocodone Bitartrate and Acetaminophen
Hydrocodone Bitartrate and Acetaminophen - 55154-9424-5 - (Hydrocodone Bitartrate and Acetaminophen)
Drug Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 55154-9424 |
| Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Non Proprietary Name: | Hydrocodone Bitartrate and Acetaminophen |
| Active Ingredient(s): | 167; 2.5 mg/5mL; mg/5mL & nbsp; Hydrocodone Bitartrate and Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocodone Bitartrate and Acetaminophen
| Product NDC: | 55154-9424 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040182 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980313 |
Package Information of Hydrocodone Bitartrate and Acetaminophen
| Package NDC: | 55154-9424-5 |
| Package Description: | 5 CUP, UNIT-DOSE in 1 BAG (55154-9424-5) > 15 mL in 1 CUP, UNIT-DOSE |
NDC Information of Hydrocodone Bitartrate and Acetaminophen
| NDC Code | 55154-9424-5 |
| Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Package Description | 5 CUP, UNIT-DOSE in 1 BAG (55154-9424-5) > 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 55154-9424 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocodone Bitartrate and Acetaminophen |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19980313 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 167; 2.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
