Package 58151-575-88

{"route": ["ORAL"], "spl_id": "fd27d2f5-1ade-4dbf-b2d2-bb98daf7da3a", "openfda": {"unii": ["UTI8907Y6X"], "rxcui": ["208149", "208161", "212233", "312938", "312940", "312941", "861064", "861066"], "spl_set_id": ["fda754f6-d0f3-4dce-a17a-927d64f912f7"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (58151-575-88)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (58151-575-32)", "package_ndc": "58151-575-88", "marketing_start_date": "20250708"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (58151-575-93)", "package_ndc": "58151-575-93", "marketing_start_date": "20250708"}], "brand_name": "Zoloft", "product_id": "58151-575_fd27d2f5-1ade-4dbf-b2d2-bb98daf7da3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "58151-575", "generic_name": "sertraline hydrochloride", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zoloft", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "NDA019839", "marketing_category": "NDA", "marketing_start_date": "20250708", "listing_expiration_date": "20261231"}