Package 29300-129-01

{"route": ["ORAL"], "spl_id": "1e92de42-a7f2-4674-8260-28cfabf0759d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0329300129014", "0329300128017"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["33f3b980-b339-4dbf-99bd-05588c2a298c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-129-01)", "package_ndc": "29300-129-01", "marketing_start_date": "20090702"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-129-05)", "package_ndc": "29300-129-05", "marketing_start_date": "20090702"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (29300-129-10)", "package_ndc": "29300-129-10", "marketing_start_date": "20090702"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (29300-129-50)", "package_ndc": "29300-129-50", "marketing_start_date": "20090702"}], "brand_name": "Hydrochlorothiazide", "product_id": "29300-129_1e92de42-a7f2-4674-8260-28cfabf0759d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "29300-129", "generic_name": "Hydrochlorothiazide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20080815", "listing_expiration_date": "20261231"}