EPOPROSTENOL .5 mg/10mL
EPOPROSTENOL · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · Mylan Institutional LLC
No Recall History
Plain English
EPOPROSTENOL is a injection, powder, lyophilized, for solution containing epoprostenol at .5 mg/10mL, taken intravenous. Manufactured by Mylan Institutional LLC.
Key Facts
- Brand Name
- EPOPROSTENOL
- Generic Name
- EPOPROSTENOL
- NDC Code (Product)
67457-587- Manufacturer
- Mylan Institutional LLC
- Strength
- .5 mg/10mL
- Dosage Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Marketing Status
- Application #
- ANDA213913
- Drug Class
- Prostacycline Vasodilator [EPC]
- Marketing Start
- 09/25/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is EPOPROSTENOL used for?
EPOPROSTENOL contains EPOPROSTENOL. It is a injection, powder, lyophilized, for solution taken intravenous. Consult your doctor for specific uses.
Is EPOPROSTENOL a controlled substance?
EPOPROSTENOL is not classified as a controlled substance by the DEA.
What is the generic name for EPOPROSTENOL?
The generic name for EPOPROSTENOL is EPOPROSTENOL. There are 7 other brand versions of EPOPROSTENOL.
What is the NDC code for EPOPROSTENOL .5 mg/10mL?
The NDC (National Drug Code) for EPOPROSTENOL .5 mg/10mL is 67457-587, listed by Mylan Institutional LLC.