Package 35573-400-99

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 35573-400-99
Digits Only 3557340099
Product NDC 35573-400
Product ID 35573-400_6752dcb1-091e-40a9-a6e2-069d543398a7
Description

1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)

Marketing

Marketing Status
Marketed Since 2018-07-13
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (1)

Finasteride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6752dcb1-091e-40a9-a6e2-069d543398a7", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0335573400996"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["c8516eaa-98d0-4eb1-bc65-aa765baea5db"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)", "package_ndc": "35573-400-99", "marketing_start_date": "20180713"}], "brand_name": "Finasteride", "product_id": "35573-400_6752dcb1-091e-40a9-a6e2-069d543398a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "35573-400", "generic_name": "Finasteride", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA203687", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}