Package 0093-5005-56

Brand: olmesartan medoxomil, amlodipine and hydrochlorothiazide

Generic: olmesartan medoxomil, amlodipine and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 0093-5005-56
Digits Only 0093500556
Product NDC 0093-5005
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-5005-56)

Marketing

Marketing Status
Marketed Since 2016-11-14
Brand olmesartan medoxomil, amlodipine and hydrochlorothiazide
Generic olmesartan medoxomil, amlodipine and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a035edd9-948f-4168-b74b-9961a2cb219a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["5c128ef2-60a6-40f3-b37f-ee139fe27987"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-5005-56)", "package_ndc": "0093-5005-56", "marketing_start_date": "20161114"}], "brand_name": "Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide", "product_id": "0093-5005_a035edd9-948f-4168-b74b-9961a2cb219a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0093-5005", "generic_name": "Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA202491", "marketing_category": "ANDA", "marketing_start_date": "20161114", "listing_expiration_date": "20261231"}