Package 67877-453-30

{"route": ["ORAL"], "spl_id": "e6461d60-f7cc-454e-b54e-2bcbcb64e631", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0367877453903", "0367877452906", "0367877451305"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["798fee33-51ad-45d0-82f3-09289304139f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67877-453-30)", "package_ndc": "67877-453-30", "marketing_start_date": "20250501"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67877-453-90)", "package_ndc": "67877-453-90", "marketing_start_date": "20250501"}], "brand_name": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "product_id": "67877-453_e6461d60-f7cc-454e-b54e-2bcbcb64e631", "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": "67877-453", "generic_name": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207037", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}