Active ingredient
Pasireotide
3 finished FDA listings contain Pasireotide as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- PASIREOTIDE
- Dosage forms
- Injection
- Routes
- Subcutaneous
- Manufacturers / labelers
- 1
- Strengths listed
- .3 mg/ml · .6 mg/ml · .9 mg/ml
- Brand names in FDA listings
- Signifor
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 1364105
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 200677 | RECORDATI RARE | 2012-12-14 | 3 |
Official labeling on DailyMed
- SIGNIFOR (PASIREOTIDE) INJECTION [RECORDATI RARE DISEASES, INC.] · version 20 · 2026-02-18
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.