Active ingredient
Anidulafungin
3 finished FDA listings contain Anidulafungin as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- ANIDULAFUNGIN
- Dosage forms
- Injection, Powder, Lyophilized, For Solution
- Routes
- Intravenous
- Manufacturers / labelers
- 1
- Strengths listed
- 100 mg/30ml · 50 mg/15ml
- Brand names in FDA listings
- Eraxis
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 341018
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 021632 | VICURON HOLDINGS | 2006-02-17 | 3 |
Official labeling on DailyMed
- ERAXIS (ANIDULAFUNGIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ROERIG] · version 24 · 2025-08-25
- ERAXIS (ANIDULAFUNGIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ROERIG] · version 2 · 2024-02-21
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.