Home
>
National Drug Code (NDC)
>
Zolvit
Zolvit - 0095-0674-16 - (hydrocodone bitartrate and acetaminophen)
Drug Information of Zolvit
| Product NDC: | 0095-0674 |
| Proprietary Name: | Zolvit |
| Non Proprietary Name: | hydrocodone bitartrate and acetaminophen |
| Active Ingredient(s): | 300; 10 mg/15mL; mg/15mL & nbsp; hydrocodone bitartrate and acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zolvit
| Product NDC: | 0095-0674 |
| Labeler Name: | ECR Pharmaceuticals Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040881 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120101 |
Package Information of Zolvit
| Package NDC: | 0095-0674-16 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0095-0674-16) |
NDC Information of Zolvit
| NDC Code | 0095-0674-16 |
| Proprietary Name | Zolvit |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0095-0674-16) |
| Product NDC | 0095-0674 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocodone bitartrate and acetaminophen |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | ANDA |
| Labeler Name | ECR Pharmaceuticals Co., Inc. |
| Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
| Strength Number | 300; 10 |
| Strength Unit | mg/15mL; mg/15mL |
| Pharmaceutical Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
