Package 42708-036-30

{"route": ["ORAL"], "spl_id": "45b3f0d0-d577-9676-e063-6394a90a5cb4", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["8d2e01fe-6d4b-4c13-a03c-77f72b635715"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["QPharma Inc"]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-036-30)", "package_ndc": "42708-036-30", "marketing_start_date": "20180314"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "42708-036_45b3f0d0-d577-9676-e063-6394a90a5cb4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "42708-036", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "QPharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA077157", "marketing_category": "ANDA", "marketing_start_date": "20100406", "listing_expiration_date": "20261231"}