ALPROSTADIL - Food and Drug Administration
- Manufacturer
- Food and Drug Administration
- Effective date
- 2014-05-08
- Label type
- Indexing - Product Concept
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-05 00:14:11
Label at a glance#
ProductALPROSTADIL
Active ingredientALPROSTADIL
Products#
Every source-derived product name is available through these pages.
- ALPROSTADIL
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALPROSTADIL | F5TD010360 | ACTIB |
| ALPROSTADIL | F5TD010360 | ACTIB |
| ALPROSTADIL | F5TD010360 | ACTIB |
| ALPROSTADIL | F5TD010360 | ACTIB |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PROSTIN VR PEDIATRIC | ALPROSTADIL | Pharmacia & Upjohn Company LLC | 930f8c02-46a8-4cff-a484-660468ab23c3 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | ALPROSTADIL |
| PROSTIN VR PEDIATRIC | ALPROSTADIL | Pharmacia & Upjohn Company LLC | dea460fa-d05e-4191-8461-f185a711ad89 | 2026-08-17 | Boxed warning, Warnings, Adverse reactions | ALPROSTADIL |
| Alprostadil | ALPROSTADIL | Meitheal Pharmaceuticals Inc. | 35d229e1-6947-435c-bf54-bfa09cca7e53 | 2024-06-04 | Boxed warning, Warnings, Adverse reactions | Alprostadil ALPROSTADIL |
| Caverject | ALPROSTADIL | Pharmacia & Upjohn Company LLC | a295fc1e-d82c-4f44-bc2d-a552bf594c98 | 2024-05-13 | Warnings, Adverse reactions | ALPROSTADIL |
| Edex | ALPROSTADIL | Endo USA, Inc. | e8b8ec8d-1318-43e4-a182-446e9f9579de | 2024-03-27 | Warnings, Adverse reactions | ALPROSTADIL |
| Caverject Impulse | ALPROSTADIL | Pharmacia & Upjohn Company LLC | 4dec1dbd-c63b-4a1b-81cb-c8d29696cc40 | 2024-02-29 | Warnings, Adverse reactions | ALPROSTADIL |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.