Package 51655-582-52

{"route": ["ORAL"], "spl_id": "494e6dd6-962e-2190-e063-6394a90a7ca5", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310818"], "spl_set_id": ["f32b8809-80e9-18f2-e053-2995a90a5428"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]", "Decreased Renal K+ Excretion [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Potassium-sparing Diuretic [EPC]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-582-26)", "package_ndc": "51655-582-26", "marketing_start_date": "20221230"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-582-52)", "package_ndc": "51655-582-52", "marketing_start_date": "20230103"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "51655-582_494e6dd6-962e-2190-e063-6394a90a7ca5", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51655-582", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamterene and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}, {"name": "TRIAMTERENE", "strength": "75 mg/1"}], "application_number": "ANDA071251", "marketing_category": "ANDA", "marketing_start_date": "20221230", "listing_expiration_date": "20271231"}