Package 68001-388-00

{"route": ["ORAL"], "spl_id": "14ca7c10-0f45-bfdf-e063-6294a90ad956", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "upc": ["0368001387002", "0368001388009"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812", "310818"], "spl_set_id": ["b8a55c23-b509-4790-88fa-9dc9bacd4bbe"], "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": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68001-388-00)", "package_ndc": "68001-388-00", "marketing_start_date": "20190618"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (68001-388-03)", "package_ndc": "68001-388-03", "marketing_start_date": "20190618"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "68001-388_14ca7c10-0f45-bfdf-e063-6294a90ad956", "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": "68001-388", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "BluePoint Laboratories", "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": "ANDA071851", "marketing_category": "ANDA", "marketing_start_date": "20190618", "listing_expiration_date": "20261231"}