losartan potassium and hydrochlorothiazide

Generic: losartan potassium and hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name losartan potassium and hydrochlorothiazide
Generic Name losartan potassium and hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1, losartan potassium 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0152
Product ID 71335-0152_d2184bfc-9552-47ce-a410-a259c0dbc7df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091629
Listing Expiration 2026-12-31
Marketing Start 2010-10-06

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350152
Hyphenated Format 71335-0152

Supplemental Identifiers

RxCUI
979468
UNII
0J48LPH2TH 3ST302B24A
NUI
N0000175359 N0000175419 M0471776

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name losartan potassium and hydrochlorothiazide (source: ndc)
Generic Name losartan potassium and hydrochlorothiazide (source: ndc)
Application Number ANDA091629 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)
  • 58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6)
  • 180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)
source: ndc

Packages (8)

71335-0152-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1) 71335-0152-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2) 71335-0152-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3) 71335-0152-4 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4) 71335-0152-5 58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5) 71335-0152-6 100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6) 71335-0152-7 180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7) 71335-0152-8 1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) losartan potassium (50 mg/1)

Linked Drug Pages (1)

Losartan Potassium and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d2184bfc-9552-47ce-a410-a259c0dbc7df", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["60f3f17d-fd28-406d-97ca-9f01f5f1c72c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1)", "package_ndc": "71335-0152-1", "marketing_start_date": "20180226"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2)", "package_ndc": "71335-0152-2", "marketing_start_date": "20240709"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3)", "package_ndc": "71335-0152-3", "marketing_start_date": "20180410"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)", "package_ndc": "71335-0152-4", "marketing_start_date": "20240709"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5)", "package_ndc": "71335-0152-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6)", "package_ndc": "71335-0152-6", "marketing_start_date": "20240709"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7)", "package_ndc": "71335-0152-7", "marketing_start_date": "20240709"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)", "package_ndc": "71335-0152-8", "marketing_start_date": "20240709"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "71335-0152_d2184bfc-9552-47ce-a410-a259c0dbc7df", "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": "71335-0152", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}