lisinopril and hydrochlorothiazide (63187-051)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler proficient rx lp

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1

Manufacturer

Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-051

Product ID 63187-051_f91a5b3e-4e83-45ec-a1a0-b815de7e1876

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076194

Listing Expiration 2026-12-31

Marketing Start 2003-03-01

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 63187051

Hyphenated Format 63187-051

Supplemental Identifiers

RxCUI

197886 197887

UPC

0363187051303 0363187050900

UNII

0J48LPH2TH E7199S1YWR

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 lisinopril and hydrochlorothiazide (source: ndc)

Generic Name lisinopril and hydrochlorothiazide (source: ndc)

Application Number ANDA076194 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
20 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE, PLASTIC (63187-051-00)
30 TABLET in 1 BOTTLE, PLASTIC (63187-051-30)
60 TABLET in 1 BOTTLE, PLASTIC (63187-051-60)
90 TABLET in 1 BOTTLE, PLASTIC (63187-051-90)

source: ndc

Packages (4)

63187-051-00 100 TABLET in 1 BOTTLE, PLASTIC (63187-051-00) 63187-051-30 30 TABLET in 1 BOTTLE, PLASTIC (63187-051-30) 63187-051-60 60 TABLET in 1 BOTTLE, PLASTIC (63187-051-60) 63187-051-90 90 TABLET in 1 BOTTLE, PLASTIC (63187-051-90)

Ingredients (2)

hydrochlorothiazide (25 mg/1) lisinopril (20 mg/1)

Linked Drug Pages (1)

Lisinopril and hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "f91a5b3e-4e83-45ec-a1a0-b815de7e1876", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0363187051303", "0363187050900"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886", "197887"], "spl_set_id": ["af0b3bef-be36-432a-884e-ea81e2d5c08e"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (63187-051-00)", "package_ndc": "63187-051-00", "marketing_start_date": "20200714"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (63187-051-30)", "package_ndc": "63187-051-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (63187-051-60)", "package_ndc": "63187-051-60", "marketing_start_date": "20200714"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (63187-051-90)", "package_ndc": "63187-051-90", "marketing_start_date": "20200714"}], "brand_name": "Lisinopril and hydrochlorothiazide", "product_id": "63187-051_f91a5b3e-4e83-45ec-a1a0-b815de7e1876", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63187-051", "generic_name": "Lisinopril and hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076194", "marketing_category": "ANDA", "marketing_start_date": "20030301", "listing_expiration_date": "20261231"}