Package 46708-149-30
Brand: olmesartan medoxomil and hydrochlorothiazide
Generic: olmesartan medoxomil and hydrochlorothiazidePackage Facts
Identity
Package NDC
46708-149-30
Digits Only
4670814930
Product NDC
46708-149
Description
30 TABLET in 1 BOTTLE (46708-149-30)
Marketing
Marketing Status
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": "b993c27f-9ada-45be-bb55-245e11564d83", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0346708149307", "0346708151300", "0346708150303"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["8c65d555-8db8-40d9-be30-309ef09f19be"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET in 1 CARTON (46708-149-08)", "package_ndc": "46708-149-08", "marketing_start_date": "20170424"}, {"sample": false, "description": "100 TABLET in 1 CARTON (46708-149-10)", "package_ndc": "46708-149-10", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-149-30)", "package_ndc": "46708-149-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (46708-149-90)", "package_ndc": "46708-149-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-149-91)", "package_ndc": "46708-149-91", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "46708-149_b993c27f-9ada-45be-bb55-245e11564d83", "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": "46708-149", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204233", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}