Package 78206-152-02

Brand: propecia

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 78206-152-02
Digits Only 7820615202
Product NDC 78206-152
Product ID 78206-152_97f5deb0-a4ab-42c3-afa0-db2170a16297
Description

90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)

Marketing

Marketing Status
Marketed Since 2021-06-01
Brand propecia
Generic finasteride
Sample Package No

Linked Drug Pages (1)

PROPECIA ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "97f5deb0-a4ab-42c3-afa0-db2170a16297", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0378206152015"], "unii": ["57GNO57U7G"], "rxcui": ["200172", "213178"], "spl_set_id": ["6f904709-65aa-44ce-b144-b4c8a0416e36"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Organon LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)", "package_ndc": "78206-152-01", "marketing_start_date": "20210601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)", "package_ndc": "78206-152-02", "marketing_start_date": "20210601"}], "brand_name": "PROPECIA", "product_id": "78206-152_97f5deb0-a4ab-42c3-afa0-db2170a16297", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "78206-152", "generic_name": "finasteride", "labeler_name": "Organon LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPECIA", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "NDA020788", "marketing_category": "NDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}