Drugplain

NDC 73302-456-01

Ella 30 mg/1

ulipristal acetate · TABLET

No Recall History

Ella is a tablet containing ulipristal acetate at a strength of 30 mg/1. Manufactured by HRA PHARMA AMERICA, INC..

Key Facts

Brand Name
Ella
Generic Name
ulipristal acetate
NDC Code (Package)
73302-456-01
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 History

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Ella — All Packages

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.