lisinopril and hydrochlorothiazide (71205-763)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide tablets

Labeler proficient rx lp

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 20 mg/1

Manufacturer

Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-763

Product ID 71205-763_84dba61d-cae2-4f21-9a9e-3088f356f838

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA076230

Listing Expiration 2026-12-31

Marketing Start 2015-03-12

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 71205763

Hyphenated Format 71205-763

Supplemental Identifiers

RxCUI

197886

UPC

0371205763305

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 tablets (source: ndc)

Application Number ANDA076230 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

12.5 mg/1
20 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE (71205-763-30)
60 TABLET in 1 BOTTLE (71205-763-60)
90 TABLET in 1 BOTTLE (71205-763-90)

source: ndc

Packages (3)

71205-763-30 30 TABLET in 1 BOTTLE (71205-763-30) 71205-763-60 60 TABLET in 1 BOTTLE (71205-763-60) 71205-763-90 90 TABLET in 1 BOTTLE (71205-763-90)

Ingredients (2)

hydrochlorothiazide (12.5 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": "84dba61d-cae2-4f21-9a9e-3088f356f838", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0371205763305"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886"], "spl_set_id": ["84dba61d-cae2-4f21-9a9e-3088f356f838"], "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 in 1 BOTTLE (71205-763-30)", "package_ndc": "71205-763-30", "marketing_start_date": "20230209"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-763-60)", "package_ndc": "71205-763-60", "marketing_start_date": "20230209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-763-90)", "package_ndc": "71205-763-90", "marketing_start_date": "20230209"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "71205-763_84dba61d-cae2-4f21-9a9e-3088f356f838", "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": "71205-763", "generic_name": "Lisinopril and Hydrochlorothiazide Tablets", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076230", "marketing_category": "ANDA", "marketing_start_date": "20150312", "listing_expiration_date": "20261231"}