Package 72189-327-90

{"route": ["ORAL"], "spl_id": "4c4c415b-609e-7934-e063-6394a90a63ba", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["d838e918-2463-79f6-e053-2a95a90a948d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-327-30)", "package_ndc": "72189-327-30", "marketing_start_date": "20220217"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-327-90)", "package_ndc": "72189-327-90", "marketing_start_date": "20220217"}], "brand_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "product_id": "72189-327_4c4c415b-609e-7934-e063-6394a90a63ba", "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": "72189-327", "generic_name": "LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE", "labeler_name": "Direct Rx", "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": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20220217", "listing_expiration_date": "20271231"}