Package 0904-6830-06

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 0904-6830-06
Digits Only 0904683006
Product NDC 0904-6830
Description

50 BLISTER PACK in 1 CARTON (0904-6830-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2015-06-13
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d1f34c55-de1d-48a5-af38-06cbea8c6b8d", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["3272651f-b500-4d5d-9e29-22fcd8e24fcb"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-6830-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6830-06", "marketing_start_date": "20150613"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6830-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6830-61", "marketing_start_date": "20150613"}], "brand_name": "Finasteride", "product_id": "0904-6830_d1f34c55-de1d-48a5-af38-06cbea8c6b8d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "0904-6830", "generic_name": "Finasteride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA090061", "marketing_category": "ANDA", "marketing_start_date": "20150613", "listing_expiration_date": "20261231"}