Package 59726-122-60

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 59726-122-60
Digits Only 5972612260
Product NDC 59726-122
Description

1 CAN in 1 PACKAGE (59726-122-60) / 60 g in 1 CAN

Marketing

Marketing Status
Marketed Since 2024-05-31
Brand minoxidil
Generic minoxidil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "69bf2912-6054-4400-a0c7-b9909ab57f1a", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0359726116022"], "unii": ["5965120SH1"], "rxcui": ["645146"], "spl_set_id": ["204bab15-47c5-449c-a889-700914b04b61"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAN in 1 PACKAGE (59726-122-60)  / 60 g in 1 CAN", "package_ndc": "59726-122-60", "marketing_start_date": "20240531"}], "brand_name": "Minoxidil", "product_id": "59726-122_69bf2912-6054-4400-a0c7-b9909ab57f1a", "dosage_form": "AEROSOL, FOAM", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "59726-122", "generic_name": "Minoxidil", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/g"}], "application_number": "ANDA208092", "marketing_category": "ANDA", "marketing_start_date": "20240531", "listing_expiration_date": "20271231"}