Package 33342-245-10
Brand: olmesartan medoxomil amlodipine and hydrochlorothiazide
Generic: olmesartan medoxomil amlodipine and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-245-10
Digits Only
3334224510
Product NDC
33342-245
Description
90 TABLET, FILM COATED in 1 BOTTLE (33342-245-10)
Marketing
Marketing Status
Brand
olmesartan medoxomil amlodipine and hydrochlorothiazide
Generic
olmesartan medoxomil amlodipine and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "52c013e1-8c31-4bed-9241-e7845873ebe8", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0333342247070", "0333342245076"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["52c013e1-8c31-4bed-9241-e7845873ebe8"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-245-07)", "package_ndc": "33342-245-07", "marketing_start_date": "20250718"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-245-10)", "package_ndc": "33342-245-10", "marketing_start_date": "20250718"}], "brand_name": "Olmesartan medoxomil Amlodipine and Hydrochlorothiazide", "product_id": "33342-245_52c013e1-8c31-4bed-9241-e7845873ebe8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "33342-245", "generic_name": "Olmesartan medoxomil Amlodipine and Hydrochlorothiazide", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan medoxomil Amlodipine and Hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207088", "marketing_category": "ANDA", "marketing_start_date": "20250718", "listing_expiration_date": "20261231"}