losartan potassium and hydrochlorothiazide (63187-599)

Drug Facts

Product Profile

Brand Name losartan potassium and hydrochlorothiazide

Generic Name losartan potassium and hydrochlorothiazide

Labeler proficient rx lp

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

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

Manufacturer

Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-599

Product ID 63187-599_c925be88-1cf9-4631-9d10-d6cca5e94765

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 63187599

Hyphenated Format 63187-599

Supplemental Identifiers

RxCUI

979468 979471

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

30 TABLET, FILM COATED in 1 BOTTLE (63187-599-30)
60 TABLET, FILM COATED in 1 BOTTLE (63187-599-60)
90 TABLET, FILM COATED in 1 BOTTLE (63187-599-90)

source: ndc

Packages (3)

63187-599-30 30 TABLET, FILM COATED in 1 BOTTLE (63187-599-30) 63187-599-60 60 TABLET, FILM COATED in 1 BOTTLE (63187-599-60) 63187-599-90 90 TABLET, FILM COATED in 1 BOTTLE (63187-599-90)

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": "c925be88-1cf9-4631-9d10-d6cca5e94765", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468", "979471"], "spl_set_id": ["198d5151-7982-4639-9fe1-6573a4529348"], "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 (63187-599-30)", "package_ndc": "63187-599-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-599-60)", "package_ndc": "63187-599-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-599-90)", "package_ndc": "63187-599-90", "marketing_start_date": "20181201"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-599_c925be88-1cf9-4631-9d10-d6cca5e94765", "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": "63187-599", "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": "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"}