Home
>
National Drug Code (NDC)
>
Ibutilide Fumarate
Ibutilide Fumarate - 10139-705-10 - (Ibutilide Fumarate)
Drug Information of Ibutilide Fumarate
| Product NDC: | 10139-705 |
| Proprietary Name: | Ibutilide Fumarate |
| Non Proprietary Name: | Ibutilide Fumarate |
| Active Ingredient(s): | .1 mg/mL & nbsp; Ibutilide Fumarate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibutilide Fumarate
| Product NDC: | 10139-705 |
| Labeler Name: | GeneraMedix Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090924 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100112 |
Package Information of Ibutilide Fumarate
| Package NDC: | 10139-705-10 |
| Package Description: | 10 mL in 1 VIAL, SINGLE-DOSE (10139-705-10) |
NDC Information of Ibutilide Fumarate
| NDC Code | 10139-705-10 |
| Proprietary Name | Ibutilide Fumarate |
| Package Description | 10 mL in 1 VIAL, SINGLE-DOSE (10139-705-10) |
| Product NDC | 10139-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ibutilide Fumarate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100112 |
| Marketing Category Name | ANDA |
| Labeler Name | GeneraMedix Inc. |
| Substance Name | IBUTILIDE FUMARATE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
