Package 33342-132-10

Brand: candesartan cilexetil and hydrochlorothiazide

Generic: candesartan cilexetil and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 33342-132-10
Digits Only 3334213210
Product NDC 33342-132
Description

90 TABLET in 1 BOTTLE (33342-132-10)

Marketing

Marketing Status
Marketed Since 2015-03-07
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 (33342-132-10)", "package_ndc": "33342-132-10", "marketing_start_date": "20150307"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-132-12)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-132-12", "marketing_start_date": "20150307"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (33342-132-15)", "package_ndc": "33342-132-15", "marketing_start_date": "20150307"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (33342-132-51)", "package_ndc": "33342-132-51", "marketing_start_date": "20150307"}], "brand_name": "Candesartan Cilexetil and Hydrochlorothiazide", "product_id": "33342-132_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": "33342-132", "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": "32 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA204100", "marketing_category": "ANDA", "marketing_start_date": "20150307", "listing_expiration_date": "20261231"}