Package 68788-8273-3

Brand: minoxidil

Generic: minoxidil
NDC Package

Package Facts

Identity

Package NDC 68788-8273-3
Digits Only 6878882733
Product NDC 68788-8273
Product ID 68788-8273_266f1046-bc25-4bcf-8002-cb11e37f20e4
Description

30 TABLET in 1 BOTTLE (68788-8273-3)

Marketing

Marketing Status
Marketed Since 2022-10-13
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": "266f1046-bc25-4bcf-8002-cb11e37f20e4", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["197987"], "spl_set_id": ["cdfd3330-4836-4655-80a2-441380529a67"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8273-3)", "package_ndc": "68788-8273-3", "marketing_start_date": "20221013"}], "brand_name": "Minoxidil", "product_id": "68788-8273_266f1046-bc25-4bcf-8002-cb11e37f20e4", "dosage_form": "TABLET", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "68788-8273", "generic_name": "Minoxidil", "labeler_name": "Preferred 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": "20221013", "listing_expiration_date": "20261231"}