Package 70436-014-06
Brand: olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Generic: olmesartan medoxomil and amlodipine besylate and hydrochlorothiazidePackage Facts
Identity
Package NDC
70436-014-06
Digits Only
7043601406
Product NDC
70436-014
Description
90 TABLET, FILM COATED in 1 BOTTLE (70436-014-06)
Marketing
Marketing Status
Brand
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Generic
olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d306cb9e-4244-49dd-9297-9cb6ca69cae9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0370436018048", "0370436016044", "0370436014040", "0370436015047", "0370436017041"], "unii": ["0J48LPH2TH", "864V2Q084H", "6M97XTV3HD"], "rxcui": ["999967", "999986", "999991", "999996", "1000001"], "spl_set_id": ["a469adff-25a6-4983-b471-60924d920a86"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70436-014-04)", "package_ndc": "70436-014-04", "marketing_start_date": "20250515"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70436-014-06)", "package_ndc": "70436-014-06", "marketing_start_date": "20250515"}], "brand_name": "olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide", "product_id": "70436-014_d306cb9e-4244-49dd-9297-9cb6ca69cae9", "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": "70436-014", "generic_name": "olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil and amlodipine besylate 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": "ANDA210718", "marketing_category": "ANDA", "marketing_start_date": "20250515", "listing_expiration_date": "20261231"}