Package 76420-154-90

{"route": ["ORAL"], "spl_id": "c8288d05-1cf2-2623-e053-2995a90a906f", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["bafe8674-b7ee-47b2-94c1-842164ca6fa1"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-154-30)", "package_ndc": "76420-154-30", "marketing_start_date": "20210728"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-154-90)", "package_ndc": "76420-154-90", "marketing_start_date": "20210728"}], "brand_name": "Finasteride", "product_id": "76420-154_c8288d05-1cf2-2623-e053-2995a90a906f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "76420-154", "generic_name": "Finasteride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA078341", "marketing_category": "ANDA", "marketing_start_date": "20071030", "listing_expiration_date": "20261231"}