Package 46708-449-10
Brand: losartan potassium and hydrochlorothiazide
Generic: losartan potassium and hydrochlorothiazidePackage Facts
Identity
Package NDC
46708-449-10
Digits Only
4670844910
Product NDC
46708-449
Description
100 BLISTER PACK in 1 CARTON (46708-449-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
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 (46708-449-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "46708-449-10", "marketing_start_date": "20160523"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (46708-449-30)", "package_ndc": "46708-449-30", "marketing_start_date": "20160523"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (46708-449-90)", "package_ndc": "46708-449-90", "marketing_start_date": "20160523"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-449-91)", "package_ndc": "46708-449-91", "marketing_start_date": "20160523"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "46708-449_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": "46708-449", "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": "100 mg/1"}], "application_number": "ANDA091617", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20261231"}