Package 57237-061-30

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 57237-061-30
Digits Only 5723706130
Product NDC 57237-061
Product ID 57237-061_2afe9ff4-1cd2-4392-8e11-8e6ea24a68af
Description

30 TABLET, FILM COATED in 1 BOTTLE (57237-061-30)

Marketing

Marketing Status
Marketed Since 2013-11-05
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": "2afe9ff4-1cd2-4392-8e11-8e6ea24a68af", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["01b88593-99d3-4dd6-a7b6-5438c15bd7b7"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (57237-061-30)", "package_ndc": "57237-061-30", "marketing_start_date": "20131105"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (57237-061-90)", "package_ndc": "57237-061-90", "marketing_start_date": "20131105"}], "brand_name": "Finasteride", "product_id": "57237-061_2afe9ff4-1cd2-4392-8e11-8e6ea24a68af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "57237-061", "generic_name": "Finasteride", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20131105", "listing_expiration_date": "20261231"}