Package 71335-2425-1
Brand: olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazidePackage Facts
Identity
Package NDC
71335-2425-1
Digits Only
7133524251
Product NDC
71335-2425
Description
90 TABLET in 1 BOTTLE (71335-2425-1)
Marketing
Marketing Status
Brand
olmesartan medoxomil and hydrochlorothiazide
Generic
olmesartan medoxomil and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "73ea2939-be63-49b4-8c95-5ae39f202f97", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403855"], "spl_set_id": ["78eb9041-a738-4056-8705-8c1dd13a4da4"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2425-1)", "package_ndc": "71335-2425-1", "marketing_start_date": "20240701"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "71335-2425_73ea2939-be63-49b4-8c95-5ae39f202f97", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-2425", "generic_name": "olmesartan medoxomil and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA207804", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}