Package 27241-302-01

{"route": ["ORAL"], "spl_id": "c1d86752-98ac-48af-8023-e57b40270660", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "W5S57Y3A5L"], "rxcui": ["866479", "866482"], "spl_set_id": ["8b78d7ad-22a8-4a9f-afb5-d18f0a4e6d36"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (27241-302-01)", "package_ndc": "27241-302-01", "marketing_start_date": "20250315"}], "brand_name": "METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE", "product_id": "27241-302_c1d86752-98ac-48af-8023-e57b40270660", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "27241-302", "generic_name": "metoprolol tartrate and hydrochlorothiazide", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOPROLOL TARTRATE AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA215789", "marketing_category": "ANDA", "marketing_start_date": "20250315", "listing_expiration_date": "20261231"}