Package 51655-311-52

{"route": ["ORAL"], "spl_id": "49d8fdcc-d10d-77cb-e063-6394a90ab6b3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886"], "spl_set_id": ["f2b94985-c79d-40e3-e053-2a95a90a0d78"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-311-26)", "package_ndc": "51655-311-26", "marketing_start_date": "20220914"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-311-52)", "package_ndc": "51655-311-52", "marketing_start_date": "20220714"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "51655-311_49d8fdcc-d10d-77cb-e063-6394a90ab6b3", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51655-311", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20220714", "listing_expiration_date": "20271231"}