Package 73302-456-01

Brand: ella

Generic: ulipristal acetate
NDC Package

Package Facts

Identity

Package NDC 73302-456-01
Digits Only 7330245601
Product NDC 73302-456
Product ID 73302-456_47d0b808-7143-c7a9-e063-6394a90a6e0d
Description

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

Marketing

Marketing Status
Marketed Since 2020-05-11
Brand ella
Generic ulipristal acetate
Sample Package No

Linked Drug Pages (1)

Ella ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47d0b808-7143-c7a9-e063-6394a90a6e0d", "openfda": {"unii": ["YF7V70N02B"], "rxcui": ["1005924", "1005928"], "spl_set_id": ["2bf93d23-cddd-4613-9066-5b5fa090404b"], "manufacturer_name": ["HRA PHARMA AMERICA, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (73302-456-01)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "73302-456-01", "marketing_start_date": "20200511"}], "brand_name": "Ella", "product_id": "73302-456_47d0b808-7143-c7a9-e063-6394a90a6e0d", "dosage_form": "TABLET", "pharm_class": ["Progesterone Agonist/Antagonist [EPC]", "Selective Progesterone Receptor Modulators [MoA]"], "product_ndc": "73302-456", "generic_name": "ulipristal acetate", "labeler_name": "HRA PHARMA AMERICA, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ella", "active_ingredients": [{"name": "ULIPRISTAL ACETATE", "strength": "30 mg/1"}], "application_number": "NDA022474", "marketing_category": "NDA", "marketing_start_date": "20200511", "listing_expiration_date": "20271231"}