Package 65862-781-78

Brand: olmesartan medoxomil and hydrochlorothiazide

Generic: olmesartan medoxomil and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 65862-781-78
Digits Only 6586278178
Product NDC 65862-781
Description

10 BLISTER PACK in 1 CARTON (65862-781-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-781-10)

Marketing

Marketing Status
Marketed Since 2017-04-24
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": "c29037bc-5702-437f-9da3-aa902291dc57", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["744c1785-42b2-46a5-b0f4-2887a9ec2051"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-781-30)", "package_ndc": "65862-781-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-781-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-781-10)", "package_ndc": "65862-781-78", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-781-90)", "package_ndc": "65862-781-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-781-99)", "package_ndc": "65862-781-99", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "65862-781_c29037bc-5702-437f-9da3-aa902291dc57", "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": "65862-781", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA205391", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}