Package 70518-2550-2

{"route": ["ORAL"], "spl_id": "4a667996-17e1-08c3-e063-6394a90ad866", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["0789baef-3424-43ab-a3fb-4908172da565"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-2550-0)", "package_ndc": "70518-2550-0", "marketing_start_date": "20200120"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2550-1)", "package_ndc": "70518-2550-1", "marketing_start_date": "20200814"}, {"sample": false, "description": "60 CAPSULE in 1 BLISTER PACK (70518-2550-2)", "package_ndc": "70518-2550-2", "marketing_start_date": "20211206"}], "brand_name": "Hydrochlorothiazide", "product_id": "70518-2550_4a667996-17e1-08c3-e063-6394a90ad866", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-2550", "generic_name": "Hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA203561", "marketing_category": "ANDA", "marketing_start_date": "20200120", "listing_expiration_date": "20271231"}