Package 49884-257-05

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 49884-257-05
Digits Only 4988425705
Product NDC 49884-257
Product ID 49884-257_d387cf20-4627-4429-8408-f240ace9df72
Description

500 TABLET in 1 BOTTLE (49884-257-05)

Marketing

Marketing Status
Marketed Since 1988-11-14
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": "d387cf20-4627-4429-8408-f240ace9df72", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0349884256012", "0349884257057"], "unii": ["5965120SH1"], "rxcui": ["197986", "197987"], "spl_set_id": ["8f3800f0-b6da-4dfe-8c32-39bb5eb0262a"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (49884-257-01)", "package_ndc": "49884-257-01", "marketing_start_date": "19881114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (49884-257-05)", "package_ndc": "49884-257-05", "marketing_start_date": "19881114"}], "brand_name": "Minoxidil", "product_id": "49884-257_d387cf20-4627-4429-8408-f240ace9df72", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "49884-257", "generic_name": "Minoxidil", "labeler_name": "Endo USA, Inc.", "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"}