Package 43393-001-06

Brand: mifepristone

Generic: mifepristone
NDC Package

Package Facts

Identity

Package NDC 43393-001-06
Digits Only 4339300106
Product NDC 43393-001
Product ID 43393-001_38fb9b4e-422b-35d9-e063-6394a90a8300
Description

6 CARTON in 1 PACKAGE (43393-001-06) / 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (43393-001-01)

Marketing

Marketing Status
Marketed Since 2019-05-01
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": "38fb9b4e-422b-35d9-e063-6394a90a8300", "openfda": {"nui": ["N0000000115", "N0000175841"], "upc": ["0343393001019", "0343393001064"], "unii": ["320T6RNW1F"], "rxcui": ["311704"], "spl_set_id": ["b63fad9b-7f12-4400-9019-b0586054e534"], "pharm_class_epc": ["Progestin Antagonist [EPC]"], "pharm_class_moa": ["Progestational Hormone Receptor Antagonists [MoA]"], "manufacturer_name": ["GenBioPro, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 CARTON in 1 PACKAGE (43393-001-06)  / 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (43393-001-01)", "package_ndc": "43393-001-06", "marketing_start_date": "20190501"}], "brand_name": "Mifepristone", "product_id": "43393-001_38fb9b4e-422b-35d9-e063-6394a90a8300", "dosage_form": "TABLET", "pharm_class": ["Progestational Hormone Receptor Antagonists [MoA]", "Progestin Antagonist [EPC]"], "product_ndc": "43393-001", "generic_name": "MIFEPRISTONE", "labeler_name": "GenBioPro, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mifepristone", "active_ingredients": [{"name": "MIFEPRISTONE", "strength": "200 mg/1"}], "application_number": "ANDA091178", "marketing_category": "ANDA", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}