Package 50090-1641-0

{"route": ["ORAL"], "spl_id": "06d80aa9-ec51-4dfa-a25e-42c20ae5ed50", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["dc9512cf-db66-40e9-afcb-1d6a722772e8"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-1641-0)", "package_ndc": "50090-1641-0", "marketing_start_date": "20150115"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1641-1)", "package_ndc": "50090-1641-1", "marketing_start_date": "20150115"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-1641-2)", "package_ndc": "50090-1641-2", "marketing_start_date": "20240802"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-1641_06d80aa9-ec51-4dfa-a25e-42c20ae5ed50", "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": "50090-1641", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20271231"}