Active ingredient
Ibutilide
3 finished FDA listings contain Ibutilide as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- IBUTILIDE FUMARATE
- Dosage forms
- Injection, Solution
- Routes
- Intravenous
- Manufacturers / labelers
- 2
- Strengths listed
- .1 mg/ml · 1 mg/10ml
- Brand names in FDA listings
- Corvert
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 41289
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| NDA 020491 | PFIZER | 1995-12-28 | 2 |
| ANDA 204146 | AVET LIFESCIENCES | 2024-04-01 | 1 |
Official labeling on DailyMed
- IBUTILIDE FUMARATE INJECTION, SOLUTION [HERITAGE PHARMACEUTICALS INC. D/B/A AVET PHARMACEUTICALS INC.] · version 5 · 2025-11-17
- CORVERT (IBUTILIDE FUMARATE) INJECTION, SOLUTION [PHARMACIA & UPJOHN COMPANY LLC] · version 9 · 2024-01-26
- CORVERT (IBUTILIDE FUMARATE) INJECTION, SOLUTION [PHARMACIA & UPJOHN COMPANY LLC] · version 11 · 2024-01-26
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.