Package 46708-448-30

Brand: losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 46708-448-30
Digits Only 4670844830
Product NDC 46708-448
Description

30 TABLET, FILM COATED in 1 BOTTLE (46708-448-30)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d80ae5dd-3bdc-40a4-9589-dfb7f8eabe6d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0346708448301", "0346708449308", "0346708450304"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["bbf7e20d-dfc2-4115-8788-c0cac15a1148"], "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": "100 BLISTER PACK in 1 CARTON (46708-448-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "46708-448-10", "marketing_start_date": "20160523"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-448-30)", "package_ndc": "46708-448-30", "marketing_start_date": "20160523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-448-90)", "package_ndc": "46708-448-90", "marketing_start_date": "20160523"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-448-91)", "package_ndc": "46708-448-91", "marketing_start_date": "20160523"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "46708-448_d80ae5dd-3bdc-40a4-9589-dfb7f8eabe6d", "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": "46708-448", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA091617", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20261231"}