Package 33342-052-12
Brand: losartan potassium and hydrochlorothiazide
Generic: losartan potassium and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-052-12
Digits Only
3334205212
Product NDC
33342-052
Description
10 BLISTER PACK in 1 CARTON (33342-052-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
losartan potassium and hydrochlorothiazide
Generic
losartan potassium and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf31d31e-9355-47da-9c2b-8e4b84ac8159", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0333342051448", "0333342050106", "0333342052100", "0333342051103", "0333342052445", "0333342051073", "0333342052070"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["a04b5622-2c49-4d61-92b1-5dc523af7a24"], "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 (33342-052-07)", "package_ndc": "33342-052-07", "marketing_start_date": "20120910"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-052-10)", "package_ndc": "33342-052-10", "marketing_start_date": "20120910"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-052-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-052-12", "marketing_start_date": "20120910"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (33342-052-44)", "package_ndc": "33342-052-44", "marketing_start_date": "20120910"}], "brand_name": "Losartan potassium and Hydrochlorothiazide", "product_id": "33342-052_cf31d31e-9355-47da-9c2b-8e4b84ac8159", "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": "33342-052", "generic_name": "Losartan potassium and Hydrochlorothiazide", "labeler_name": "Macleods Pharmaceuticals Limited", "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": "ANDA202289", "marketing_category": "ANDA", "marketing_start_date": "20120503", "listing_expiration_date": "20261231"}