Package 60505-2656-5

{"route": ["ORAL"], "spl_id": "2b178a53-cddb-a0e3-2eb7-752e47edc56a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "upc": ["0360505265619", "0360505265718"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812", "310818"], "spl_set_id": ["bd6c3495-ec70-908b-482a-a979506659e9"], "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": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (60505-2656-1)", "package_ndc": "60505-2656-1", "marketing_start_date": "20090921"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (60505-2656-5)", "package_ndc": "60505-2656-5", "marketing_start_date": "20090921"}, {"sample": false, "description": "6500 TABLET in 1 BOTTLE (60505-2656-7)", "package_ndc": "60505-2656-7", "marketing_start_date": "20090921"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "60505-2656_2b178a53-cddb-a0e3-2eb7-752e47edc56a", "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": "60505-2656", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Apotex Corp.", "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": "20090921", "listing_expiration_date": "20271231"}