Package 33342-131-12
Brand: candesartan cilexetil and hydrochlorothiazide
Generic: candesartan cilexetil and hydrochlorothiazidePackage Facts
Identity
Package NDC
33342-131-12
Digits Only
3334213112
Product NDC
33342-131
Description
10 BLISTER PACK in 1 CARTON (33342-131-12) / 10 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
candesartan cilexetil and hydrochlorothiazide
Generic
candesartan cilexetil and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "66ca941e-6590-41a6-8d8f-caa2013089d0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0333342133106", "0333342131515", "0333342132109", "0333342131102"], "unii": ["0J48LPH2TH", "R85M2X0D68"], "rxcui": ["578325", "578330", "802749"], "spl_set_id": ["76630807-9717-44be-946d-756038cf677e"], "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": "90 TABLET in 1 BOTTLE (33342-131-10)", "package_ndc": "33342-131-10", "marketing_start_date": "20150307"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-131-12) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-131-12", "marketing_start_date": "20150307"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (33342-131-15)", "package_ndc": "33342-131-15", "marketing_start_date": "20150307"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (33342-131-51)", "package_ndc": "33342-131-51", "marketing_start_date": "20150307"}], "brand_name": "Candesartan Cilexetil and Hydrochlorothiazide", "product_id": "33342-131_66ca941e-6590-41a6-8d8f-caa2013089d0", "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": "33342-131", "generic_name": "Candesartan Cilexetil and Hydrochlorothiazide", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Candesartan Cilexetil and Hydrochlorothiazide", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "16 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA204100", "marketing_category": "ANDA", "marketing_start_date": "20150307", "listing_expiration_date": "20261231"}