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Corvert
Corvert - 0009-3794-22 - (IBUTILIDE FUMARATE)
Drug Information of Corvert
| Product NDC: | 0009-3794 |
| Proprietary Name: | Corvert |
| 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 Corvert
| Product NDC: | 0009-3794 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020491 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951228 |
Package Information of Corvert
| Package NDC: | 0009-3794-22 |
| Package Description: | 10 mL in 1 VIAL, SINGLE-DOSE (0009-3794-22) |
NDC Information of Corvert
| NDC Code | 0009-3794-22 |
| Proprietary Name | Corvert |
| Package Description | 10 mL in 1 VIAL, SINGLE-DOSE (0009-3794-22) |
| Product NDC | 0009-3794 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | IBUTILIDE FUMARATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19951228 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | IBUTILIDE FUMARATE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
