Package 62332-050-10

Brand: losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 62332-050-10
Digits Only 6233205010
Product NDC 62332-050
Description

100 BLISTER PACK in 1 CARTON (62332-050-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2016-05-23
Brand losartan potassium and hydrochlorothiazide
Generic losartan potassium and hydrochlorothiazide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a9657dc9-2be3-4719-a5b7-fbf22603275e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362332048304", "0362332050307", "0362332049301"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["acecced9-2a61-435d-b7d4-b151cb7b7e5d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62332-050-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62332-050-10", "marketing_start_date": "20160523"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-050-30)", "package_ndc": "62332-050-30", "marketing_start_date": "20160523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-050-90)", "package_ndc": "62332-050-90", "marketing_start_date": "20160523"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-050-91)", "package_ndc": "62332-050-91", "marketing_start_date": "20160523"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "62332-050_a9657dc9-2be3-4719-a5b7-fbf22603275e", "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": "62332-050", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091617", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20271231"}