Package 71713-099-90
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
71713-099-90
Digits Only
7171309990
Product NDC
71713-099
Description
90 TABLET in 1 CONTAINER (71713-099-90)
Marketing
Marketing Status
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": "3fe7bdaa-b027-4da9-94ee-550bf28c63e1", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["3fe7bdaa-b027-4da9-94ee-550bf28c63e1"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Thirty Madison Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 CONTAINER (71713-099-90)", "package_ndc": "71713-099-90", "marketing_start_date": "20210322"}], "brand_name": "Finasteride", "product_id": "71713-099_3fe7bdaa-b027-4da9-94ee-550bf28c63e1", "dosage_form": "TABLET", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "71713-099", "generic_name": "Finasteride", "labeler_name": "Thirty Madison Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA207750", "marketing_category": "ANDA", "marketing_start_date": "20210322", "listing_expiration_date": "20261231"}