Package 0378-0434-01

{"route": ["ORAL"], "spl_id": "771d61ce-0810-4998-b77b-9d3fe58056d9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0303780434011", "0303780424012", "0303780445017"], "unii": ["0J48LPH2TH", "W5S57Y3A5L"], "rxcui": ["866479", "866482", "866491"], "spl_set_id": ["b6cf0f43-8dc3-4535-b651-daf1f9e0336c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-0434-01)", "package_ndc": "0378-0434-01", "marketing_start_date": "20040820"}], "brand_name": "Metoprolol Tartrate and Hydrochlorothiazide", "product_id": "0378-0434_771d61ce-0810-4998-b77b-9d3fe58056d9", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0378-0434", "generic_name": "metoprolol tartrate and hydrochlorothiazide", "labeler_name": "Mylan Pharmaceuticals 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": "ANDA076792", "marketing_category": "ANDA", "marketing_start_date": "20040820", "listing_expiration_date": "20261231"}