Package 0591-4390-96

Brand: mifepristone

Generic: mifepristone
NDC Package

Package Facts

Identity

Package NDC 0591-4390-96
Digits Only 0591439096
Product NDC 0591-4390
Product ID 0591-4390_57067545-4dd0-4ab0-ba97-d17d74fe7d69
Description

28 TABLET, FILM COATED in 1 BOTTLE (0591-4390-96)

Marketing

Marketing Status
Marketed Since 2024-01-19
Brand mifepristone
Generic mifepristone
Sample Package No

Linked Drug Pages (1)

Mifepristone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "57067545-4dd0-4ab0-ba97-d17d74fe7d69", "openfda": {"nui": ["N0000000115", "N0000175841"], "upc": ["0305914390965"], "unii": ["320T6RNW1F"], "rxcui": ["1245262"], "spl_set_id": ["5e09acc0-fd26-4722-b8b3-46e560390d47"], "pharm_class_epc": ["Progestin Antagonist [EPC]"], "pharm_class_moa": ["Progestational Hormone Receptor Antagonists [MoA]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (0591-4390-96)", "package_ndc": "0591-4390-96", "marketing_start_date": "20240119"}], "brand_name": "Mifepristone", "product_id": "0591-4390_57067545-4dd0-4ab0-ba97-d17d74fe7d69", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Progestational Hormone Receptor Antagonists [MoA]", "Progestin Antagonist [EPC]"], "product_ndc": "0591-4390", "generic_name": "Mifepristone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mifepristone", "active_ingredients": [{"name": "MIFEPRISTONE", "strength": "300 mg/1"}], "application_number": "ANDA211436", "marketing_category": "ANDA", "marketing_start_date": "20240119", "listing_expiration_date": "20261231"}