Corvert is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Pharmacia & Upjohn Company Llc. The primary component is Ibutilide Fumarate.
| Product ID | 0009-3794_13e6540f-3b41-4480-a729-c6cc78b59ca6 |
| NDC | 0009-3794 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Corvert |
| Generic Name | Ibutilide Fumarate |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 1995-12-28 |
| Marketing Category | NDA / NDA |
| Application Number | NDA020491 |
| Labeler Name | Pharmacia & Upjohn Company LLC |
| Substance Name | IBUTILIDE FUMARATE |
| Active Ingredient Strength | 0 mg/mL |
| Pharm Classes | Antiarrhythmic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 1995-12-28 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA020491 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-12-28 |
| Marketing Category | NDA |
| Application Number | NDA020491 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1995-12-28 |
| Marketing Category | NDA |
| Application Number | NDA020491 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-12-28 |
| Marketing End Date | 2011-12-01 |
| Ingredient | Strength |
|---|---|
| IBUTILIDE FUMARATE | .1 mg/mL |
| SPL SET ID: | 2428969a-7431-4e94-9503-ad5c680e2ea4 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0009-3794 | Corvert | ibutilide fumarate |
| 67457-366 | Ibutilide Fumarate | Ibutilide Fumarate |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CORVERT 74469537 2027397 Live/Registered |
PHARMACIA & UPJOHN COMPANY LLC 1993-12-14 |