Package 49884-788-09

Brand: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide

Generic: olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 49884-788-09
Digits Only 4988478809
Product NDC 49884-788
Description

90 TABLET, FILM COATED in 1 BOTTLE (49884-788-09)

Marketing

Marketing Status
Marketed Since 2016-10-26
Brand olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Generic olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "64db5fb3-c133-422f-9cf5-98e60d98bdc4", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0349884787097", "0349884788094", "0349884786090", "0349884789091", "0349884790097"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["268d12e8-1cfc-4086-b613-8fd94f2d7c4e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (49884-788-09)", "package_ndc": "49884-788-09", "marketing_start_date": "20161026"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (49884-788-11)", "package_ndc": "49884-788-11", "marketing_start_date": "20161026"}], "brand_name": "olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide", "product_id": "49884-788_64db5fb3-c133-422f-9cf5-98e60d98bdc4", "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": "49884-788", "generic_name": "olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA206137", "marketing_category": "ANDA", "marketing_start_date": "20161026", "listing_expiration_date": "20261231"}