Ella 30 mg/1
ulipristal acetate · TABLET · HRA PHARMA AMERICA, INC.
No Recall History
Plain English
Ella is a tablet containing ulipristal acetate at 30 mg/1, taken oral. Manufactured by HRA PHARMA AMERICA, INC..
Key Facts
- Brand Name
- Ella
- Generic Name
- ulipristal acetate
- NDC Code (Product)
73302-456- Manufacturer
- HRA PHARMA AMERICA, INC.
- Strength
- 30 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA022474
- Marketing Start
- 05/11/2020
Recall History
No Recall HistoryFrequently Asked Questions
What is Ella used for?
Ella contains ulipristal acetate. It is a tablet taken oral. Consult your doctor for specific uses.
Is Ella a controlled substance?
Ella is not classified as a controlled substance by the DEA.
What is the generic name for Ella?
The generic name for Ella is ulipristal acetate. There are no other listed brand versions of ulipristal acetate.
What is the NDC code for Ella 30 mg/1?
The NDC (National Drug Code) for Ella 30 mg/1 is 73302-456, listed by HRA PHARMA AMERICA, INC..
Other Ella Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)