Package 0555-0483-05

{"route": ["ORAL"], "spl_id": "3c6d3a11-6d0b-4109-89cd-658827847fea", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["FZJ37245UC", "0J48LPH2TH"], "rxcui": ["977883"], "spl_set_id": ["8b2c581a-f955-4a8e-bf85-e768e903fd10"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0555-0483-02)", "package_ndc": "0555-0483-02", "marketing_start_date": "19891201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0555-0483-05)", "package_ndc": "0555-0483-05", "marketing_start_date": "19891201"}], "brand_name": "Amiloride Hydrochloride and Hydrochlorothiazide", "product_id": "0555-0483_3c6d3a11-6d0b-4109-89cd-658827847fea", "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": "0555-0483", "generic_name": "Amiloride Hydrochloride and Hydrochlorothiazide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amiloride Hydrochloride and Hydrochlorothiazide", "active_ingredients": [{"name": "AMILORIDE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA071111", "marketing_category": "ANDA", "marketing_start_date": "19891201", "listing_expiration_date": "20261231"}