Package 33342-173-44
Brand: olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-173-44
Digits Only
3334217344
Product NDC
33342-173
Description
1000 TABLET, FILM COATED in 1 BOTTLE (33342-173-44)
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": "79da177b-5eeb-4d95-b949-251b7e8c948b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0333342175076", "0333342173102", "0333342173447", "0333342175441", "0333342174079", "0333342174109", "0333342173072", "0333342175106", "0333342174444"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["03ff0f7e-6aa1-4c38-8c9a-5f1c6a56c747"], "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 (33342-173-07)", "package_ndc": "33342-173-07", "marketing_start_date": "20230602"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-173-10)", "package_ndc": "33342-173-10", "marketing_start_date": "20230602"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-173-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-173-12", "marketing_start_date": "20230602"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (33342-173-44)", "package_ndc": "33342-173-44", "marketing_start_date": "20230602"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "33342-173_79da177b-5eeb-4d95-b949-251b7e8c948b", "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": "33342-173", "generic_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "labeler_name": "Macleods Pharmaceuticals Limited", "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": "ANDA204801", "marketing_category": "ANDA", "marketing_start_date": "20230602", "listing_expiration_date": "20261231"}