Package 17856-0090-1

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 17856-0090-1
Digits Only 1785600901
Product NDC 17856-0090
Description

1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)

Marketing

Marketing Status
Marketed Since 2021-01-11
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": "385463d5-f3d9-96c0-e063-6294a90ac25e", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["29e59387-120c-4367-9f87-75cb53b6460d"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Atlantic Biologicals Corps"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)", "package_ndc": "17856-0090-1", "marketing_start_date": "20210111"}], "brand_name": "Finasteride", "product_id": "17856-0090_385463d5-f3d9-96c0-e063-6294a90ac25e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "17856-0090", "generic_name": "finasteride", "labeler_name": "Atlantic Biologicals Corps", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA090121", "marketing_category": "ANDA", "marketing_start_date": "20100528", "listing_expiration_date": "20261231"}