Package 70771-1327-1

Brand: candesartan cilexetil and hydrochlorothiazide

Generic: candesartan cilexetil and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 70771-1327-1
Digits Only 7077113271
Product NDC 70771-1327
Description

100 TABLET in 1 BOTTLE (70771-1327-1)

Marketing

Marketing Status
Marketed Since 2018-04-14
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": "2b38d778-d732-4a7b-bb34-b426a14e10bc", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "R85M2X0D68"], "rxcui": ["578325", "578330", "802749"], "spl_set_id": ["cb328bc1-5738-4620-b2b3-442e98388a86"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1327-0)", "package_ndc": "70771-1327-0", "marketing_start_date": "20180414"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1327-1)", "package_ndc": "70771-1327-1", "marketing_start_date": "20180414"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70771-1327-3)", "package_ndc": "70771-1327-3", "marketing_start_date": "20180414"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1327-4)  / 10 TABLET in 1 BLISTER PACK (70771-1327-2)", "package_ndc": "70771-1327-4", "marketing_start_date": "20180414"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1327-9)", "package_ndc": "70771-1327-9", "marketing_start_date": "20180414"}], "brand_name": "candesartan cilexetil and hydrochlorothiazide", "product_id": "70771-1327_2b38d778-d732-4a7b-bb34-b426a14e10bc", "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": "70771-1327", "generic_name": "candesartan cilexetil and hydrochlorothiazide", "labeler_name": "Zydus Lifesciences 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": "25 mg/1"}], "application_number": "ANDA203466", "marketing_category": "ANDA", "marketing_start_date": "20180414", "listing_expiration_date": "20261231"}