Package 53489-386-01

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 53489-386-01
Digits Only 5348938601
Product NDC 53489-386
Description

100 TABLET in 1 BOTTLE (53489-386-01)

Marketing

Marketing Status
Marketed Since 1995-12-14
Brand minoxidil
Generic minoxidil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a668fcd-612e-6944-e063-6394a90a9e2f", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197986", "197987"], "spl_set_id": ["0354a7f5-5917-44dc-9963-411104008cb5"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53489-386-01)", "package_ndc": "53489-386-01", "marketing_start_date": "19951214"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (53489-386-03)", "package_ndc": "53489-386-03", "marketing_start_date": "19951214"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53489-386-05)", "package_ndc": "53489-386-05", "marketing_start_date": "19951214"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53489-386-10)", "package_ndc": "53489-386-10", "marketing_start_date": "19951214"}], "brand_name": "MINOXIDIL", "product_id": "53489-386_4a668fcd-612e-6944-e063-6394a90a9e2f", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "53489-386", "generic_name": "minoxidil", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MINOXIDIL", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA072709", "marketing_category": "ANDA", "marketing_start_date": "19951214", "listing_expiration_date": "20271231"}