Package 68071-3794-3

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 68071-3794-3
Digits Only 6807137943
Product NDC 68071-3794
Product ID 68071-3794_48862260-1894-0602-e063-6294a90a1eff
Description

30 TABLET in 1 BOTTLE (68071-3794-3)

Marketing

Marketing Status
Marketed Since 2025-02-17
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": "48862260-1894-0602-e063-6294a90a1eff", "openfda": {"nui": ["N0000175379", "N0000175564"], "upc": ["0368071379433"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["2e5a2976-06fb-43f9-e063-6294a90a3bf5"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3794-3)", "package_ndc": "68071-3794-3", "marketing_start_date": "20250217"}], "brand_name": "Minoxidil", "product_id": "68071-3794_48862260-1894-0602-e063-6294a90a1eff", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68071-3794", "generic_name": "Minoxidil", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "2.5 mg/1"}], "application_number": "ANDA071826", "marketing_category": "ANDA", "marketing_start_date": "19881114", "listing_expiration_date": "20271231"}