Package 51655-630-26

{"route": ["ORAL"], "spl_id": "494f3f77-4b1b-4cb1-e063-6294a90aaa1e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["9ec3d35f-b25d-48f4-926f-f093e402ccde"], "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 (51655-630-26)", "package_ndc": "51655-630-26", "marketing_start_date": "20210521"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, DISPENSING (51655-630-52)", "package_ndc": "51655-630-52", "marketing_start_date": "20140407"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "51655-630_494f3f77-4b1b-4cb1-e063-6294a90aaa1e", "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": "51655-630", "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": "ANDA071251", "marketing_category": "ANDA", "marketing_start_date": "20140407", "listing_expiration_date": "20271231"}