Package 70010-188-03

{"route": ["ORAL"], "spl_id": "1cb60a8e-0849-4a3e-e063-6294a90a350e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0370010188037", "0370010189034"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["b4168479-09ec-402c-89cc-456bc8485017"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70010-188-03)", "package_ndc": "70010-188-03", "marketing_start_date": "20230929"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70010-188-10)", "package_ndc": "70010-188-10", "marketing_start_date": "20230929"}], "brand_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "product_id": "70010-188_1cb60a8e-0849-4a3e-e063-6294a90a350e", "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": "70010-188", "generic_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "labeler_name": "Granules Pharmaceuticals 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": "100 mg/1"}], "application_number": "ANDA218015", "marketing_category": "ANDA", "marketing_start_date": "20230929", "listing_expiration_date": "20261231"}