Package 84670-014-01

Brand: mifepristone

Generic: mifepristone
NDC Package

Package Facts

Identity

Package NDC 84670-014-01
Digits Only 8467001401
Product NDC 84670-014
Description

1 TABLET in 1 BLISTER PACK (84670-014-01)

Marketing

Marketing Status
Marketed Since 2025-09-30
Brand mifepristone
Generic mifepristone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b7d82f9-da40-ce2e-e063-6294a90a92fd", "openfda": {"nui": ["N0000000115", "N0000175841"], "upc": ["0384670014018"], "unii": ["320T6RNW1F"], "rxcui": ["311704"], "spl_set_id": ["839d7a7d-de19-42bd-8810-132b3c2a5daf"], "pharm_class_epc": ["Progestin Antagonist [EPC]"], "pharm_class_moa": ["Progestational Hormone Receptor Antagonists [MoA]"], "manufacturer_name": ["Evita Solutions LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 BLISTER PACK (84670-014-01)", "package_ndc": "84670-014-01", "marketing_start_date": "20250930"}], "brand_name": "Mifepristone", "product_id": "84670-014_4b7d82f9-da40-ce2e-e063-6294a90a92fd", "dosage_form": "TABLET", "pharm_class": ["Progestational Hormone Receptor Antagonists [MoA]", "Progestin Antagonist [EPC]"], "product_ndc": "84670-014", "generic_name": "MIFEPRISTONE", "labeler_name": "Evita Solutions LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mifepristone", "active_ingredients": [{"name": "MIFEPRISTONE", "strength": "200 mg/1"}], "application_number": "ANDA216616", "marketing_category": "ANDA", "marketing_start_date": "20250930", "listing_expiration_date": "20271231"}