Package 63187-347-60

Brand: losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 63187-347-60
Digits Only 6318734760
Product NDC 63187-347
Description

60 TABLET, FILM COATED in 1 BOTTLE (63187-347-60)

Marketing

Marketing Status
Marketed Since 2023-08-21
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": "6bff4e15-4418-45b5-8c30-2ff825249f9c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0363187347307"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["8d992a4c-8740-4636-928f-bb808eae3336"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-347-30)", "package_ndc": "63187-347-30", "marketing_start_date": "20230821"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-347-60)", "package_ndc": "63187-347-60", "marketing_start_date": "20230821"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-347-90)", "package_ndc": "63187-347-90", "marketing_start_date": "20230821"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-347_6bff4e15-4418-45b5-8c30-2ff825249f9c", "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": "63187-347", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "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": "ANDA077157", "marketing_category": "ANDA", "marketing_start_date": "20100406", "listing_expiration_date": "20261231"}