Package 33342-173-12
Brand: olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-173-12
Digits Only
3334217312
Product NDC
33342-173
Description
10 BLISTER PACK in 1 CARTON (33342-173-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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"}