Package 72162-1490-5

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 72162-1490-5
Digits Only 7216214905
Product NDC 72162-1490
Product ID 72162-1490_04276eed-6d51-6906-e063-6294a90a5a06
Description

500 TABLET in 1 BOTTLE (72162-1490-5)

Marketing

Marketing Status
Marketed Since 2023-04-21
Brand minoxidil
Generic minoxidil
Sample Package No

Linked Drug Pages (1)

Minoxidil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "04276eed-6d51-6906-e063-6294a90a5a06", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197986"], "spl_set_id": ["665cba3d-5f26-468a-a047-188a413fbede"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1490-5)", "package_ndc": "72162-1490-5", "marketing_start_date": "20230421"}], "brand_name": "Minoxidil", "product_id": "72162-1490_04276eed-6d51-6906-e063-6294a90a5a06", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "72162-1490", "generic_name": "Minoxidil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "10 mg/1"}], "application_number": "ANDA071839", "marketing_category": "ANDA", "marketing_start_date": "19881114", "listing_expiration_date": "20261231"}