Package 68462-879-01

{"route": ["ORAL"], "spl_id": "6154a348-821d-46cc-a830-ac5684f9525a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368462880302", "0368462879306", "0368462878309"], "unii": ["0J48LPH2TH", "UR59KN573L"], "rxcui": ["854908", "854916", "854919"], "spl_set_id": ["ab73a6d8-2e33-4fdc-a896-6c68ab772da6"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["GLENMARK PHARMACEUTICALS INC., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-879-01)", "package_ndc": "68462-879-01", "marketing_start_date": "20220126"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68462-879-05)", "package_ndc": "68462-879-05", "marketing_start_date": "20220126"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-879-30)", "package_ndc": "68462-879-30", "marketing_start_date": "20220126"}], "brand_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "product_id": "68462-879_6154a348-821d-46cc-a830-ac5684f9525a", "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": "68462-879", "generic_name": "Bisoprolol Fumarate and Hydrochlorothiazide", "labeler_name": "GLENMARK PHARMACEUTICALS INC., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bisoprolol Fumarate and Hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA215995", "marketing_category": "ANDA", "marketing_start_date": "20220126", "listing_expiration_date": "20271231"}