Package 82868-006-30

{"route": ["ORAL"], "spl_id": "46dc8d44-ebc1-6013-e063-6294a90a11f7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["03b11335-2e88-2f7b-e063-6394a90afe2a"], "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": "30 TABLET in 1 BOTTLE, PLASTIC (82868-006-30)", "package_ndc": "82868-006-30", "marketing_start_date": "20230818"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-006-90)", "package_ndc": "82868-006-90", "marketing_start_date": "20230825"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "82868-006_46dc8d44-ebc1-6013-e063-6294a90a11f7", "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": "82868-006", "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": "25 mg/1"}, {"name": "TRIAMTERENE", "strength": "37.5 mg/1"}], "application_number": "ANDA216211", "marketing_category": "ANDA", "marketing_start_date": "20230818", "listing_expiration_date": "20261231"}