Package 71335-1931-1

{"route": ["ORAL"], "spl_id": "206c9b1f-f95a-4cc9-a1fa-69d2a2213391", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["UR59KN573L", "0J48LPH2TH"], "rxcui": ["854916"], "spl_set_id": ["53221419-204c-40a2-9ec3-8e4b994dd39d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1931-1)", "package_ndc": "71335-1931-1", "marketing_start_date": "20240408"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1931-2)", "package_ndc": "71335-1931-2", "marketing_start_date": "20210806"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1931-3)", "package_ndc": "71335-1931-3", "marketing_start_date": "20240408"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "71335-1931_206c9b1f-f95a-4cc9-a1fa-69d2a2213391", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1931", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA212678", "marketing_category": "ANDA", "marketing_start_date": "20190430", "listing_expiration_date": "20261231"}