Package 29300-187-05

{"route": ["ORAL"], "spl_id": "057844aa-5d7e-4e83-b71f-9072d2a2b93d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "UR59KN573L"], "rxcui": ["854908", "854916", "854919"], "spl_set_id": ["b9ee689a-ea12-435d-b01c-70d45891e62f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (29300-187-01)", "package_ndc": "29300-187-01", "marketing_start_date": "20101012"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (29300-187-05)", "package_ndc": "29300-187-05", "marketing_start_date": "20101012"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (29300-187-10)", "package_ndc": "29300-187-10", "marketing_start_date": "20101012"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (29300-187-13)", "package_ndc": "29300-187-13", "marketing_start_date": "20101012"}], "brand_name": "bisoprolol fumarate and hydrochlorothiazide", "product_id": "29300-187_057844aa-5d7e-4e83-b71f-9072d2a2b93d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-187", "generic_name": "bisoprolol fumarate and hydrochlorothiazide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bisoprolol fumarate and hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "2.5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA079106", "marketing_category": "ANDA", "marketing_start_date": "20101012", "listing_expiration_date": "20261231"}