Package 72789-512-30

{"route": ["ORAL"], "spl_id": "44086807-4be4-f324-e063-6394a90a0c49", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372789512303"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["c182b6a9-1a31-45ee-9cea-a557c99f5db7"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30)", "package_ndc": "72789-512-30", "marketing_start_date": "20250606"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60)", "package_ndc": "72789-512-60", "marketing_start_date": "20251029"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)", "package_ndc": "72789-512-90", "marketing_start_date": "20250606"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-512_44086807-4be4-f324-e063-6394a90a0c49", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-512", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19730112", "listing_expiration_date": "20261231"}