Package 70518-2287-0
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
70518-2287-0
Digits Only
7051822870
Product NDC
70518-2287
Description
90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2287-0)
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": "49f0e8c7-5ef3-a410-e063-6294a90a45ef", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["90cc0d22-fa5c-4fe4-b0bf-554b715a05ac"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2287-0)", "package_ndc": "70518-2287-0", "marketing_start_date": "20190827"}], "brand_name": "Finasteride", "product_id": "70518-2287_49f0e8c7-5ef3-a410-e063-6294a90a45ef", "dosage_form": "TABLET, COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "70518-2287", "generic_name": "Finasteride", "labeler_name": "REMEDYREPACK 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": "20190827", "listing_expiration_date": "20271231"}