Package 42658-141-07

{"route": ["ORAL"], "spl_id": "2ca630bf-9b77-9da8-e063-6294a90a87b9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0342658142016", "0342658141019"], "unii": ["0J48LPH2TH", "J0E2756Z7N"], "rxcui": ["310792", "310793"], "spl_set_id": ["e6d11cd6-7204-4031-a6c5-8f6a33568ab4"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Hisun Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42658-141-01)", "package_ndc": "42658-141-01", "marketing_start_date": "20250101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42658-141-04)", "package_ndc": "42658-141-04", "marketing_start_date": "20250101"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42658-141-07)", "package_ndc": "42658-141-07", "marketing_start_date": "20250101"}], "brand_name": "IRBESARTAN AND HYDROCHLOROTHIAZIDE", "product_id": "42658-141_2ca630bf-9b77-9da8-e063-6294a90a87b9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "42658-141", "generic_name": "irbesartan and hydrochlorothiazide", "labeler_name": "Hisun Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IRBESARTAN AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "IRBESARTAN", "strength": "150 mg/1"}], "application_number": "ANDA207896", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}