Package 69315-155-01

{"route": ["ORAL"], "spl_id": "001b600e-a6f4-4f39-bdd3-cf29fb96fa83", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0369315131107", "0369315131503", "0369315130100", "0369315155103"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["8c868894-667e-4a51-906a-838d63e420ba"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (69315-155-01)", "package_ndc": "69315-155-01", "marketing_start_date": "20191101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (69315-155-10)", "package_ndc": "69315-155-10", "marketing_start_date": "20191101"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "69315-155_001b600e-a6f4-4f39-bdd3-cf29fb96fa83", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "69315-155", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}