NDC 73302-456

Ella

Ulipristal Acetate

Ella is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Hra Pharma America, Inc.. The primary component is Ulipristal Acetate.

Product ID73302-456_ec302ec7-b606-4eae-b35d-e51e67312aac
NDC73302-456
Product TypeHuman Prescription Drug
Proprietary NameElla
Generic NameUlipristal Acetate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2020-05-11
Marketing CategoryNDA / NDA
Application NumberNDA022474
Labeler NameHRA Pharma America, Inc.
Substance NameULIPRISTAL ACETATE
Active Ingredient Strength30 mg/1
Pharm ClassesProgesterone Agonist/Antagonist [EPC],Selective Progesterone Receptor Modulators [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 73302-456-01

1 BLISTER PACK in 1 CARTON (73302-456-01) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2020-05-11
NDC Exclude FlagN
Sample Package?N

Drug Details

Active Ingredients

IngredientStrength
ULIPRISTAL ACETATE30 mg/1

NDC Crossover Matching brand name "Ella" or generic name "Ulipristal Acetate"

NDCBrand NameGeneric Name
50090-2835Ellaulipristal acetate
50102-911Ellaulipristal acetate
53002-1630Ellaulipristal acetate
73302-456Ellaulipristal acetate

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