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 ID: 73302-456_ec302ec7-b606-4eae-b35d-e51e67312aac
• NDC: 73302-456
• Product Type: Human Prescription Drug
• Proprietary Name: Ella
• Generic Name: Ulipristal Acetate
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2020-05-11
• Marketing Category: NDA / NDA
• Application Number: NDA022474
• Labeler Name: HRA Pharma America, Inc.
• Substance Name: ULIPRISTAL ACETATE
• Active Ingredient Strength: 30 mg/1
• Pharm Classes: Progesterone Agonist/Antagonist [EPC],Selective Progesterone Receptor Modulators [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 73302-456-01

1 BLISTER PACK in 1 CARTON (73302-456-01) > 1 TABLET in 1 BLISTER PACK

• Marketing Start Date: 2020-05-11
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73302-456-01 [73302045601]

Ella TABLET

• Marketing Category: NDA
• Application Number: NDA022474
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-05-11

Drug Details

Active Ingredients

Ingredient	Strength
ULIPRISTAL ACETATE	30 mg/1

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

NDC	Brand Name	Generic Name
50090-2835	Ella	ulipristal acetate
50090-5422	Ella	ulipristal acetate
50102-911	Ella	ulipristal acetate
53002-1630	Ella	ulipristal acetate
53002-2630	Ella	ulipristal acetate
73302-456	Ella	ulipristal acetate
82454-0456	Ella	ulipristal acetate