lisinopril and hydrochlorothiazide (68071-3008)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler nucarepharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 10 mg/1

Manufacturer

NuCarePharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3008

Product ID 68071-3008_1d788f31-9c44-5af1-e063-6394a90a0a5b

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 680713008

Hyphenated Format 68071-3008

Supplemental Identifiers

RxCUI

197885

UPC

0368071300895

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

12.5 mg/1
10 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE (68071-3008-3)
60 TABLET in 1 BOTTLE (68071-3008-6)
90 TABLET in 1 BOTTLE (68071-3008-9)

source: ndc

Packages (3)

68071-3008-3 30 TABLET in 1 BOTTLE (68071-3008-3) 68071-3008-6 60 TABLET in 1 BOTTLE (68071-3008-6) 68071-3008-9 90 TABLET in 1 BOTTLE (68071-3008-9)

Ingredients (2)

hydrochlorothiazide (12.5 mg/1) lisinopril (10 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": "1d788f31-9c44-5af1-e063-6394a90a0a5b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071300895"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885"], "spl_set_id": ["4fbf31a1-037b-31a2-e054-00144ff88e88"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCarePharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3008-3)", "package_ndc": "68071-3008-3", "marketing_start_date": "20170517"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3008-6)", "package_ndc": "68071-3008-6", "marketing_start_date": "20170517"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3008-9)", "package_ndc": "68071-3008-9", "marketing_start_date": "20170517"}], "brand_name": "Lisinopril and hydrochlorothiazide", "product_id": "68071-3008_1d788f31-9c44-5af1-e063-6394a90a0a5b", "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": "68071-3008", "generic_name": "Lisinopril and hydrochlorothiazide", "labeler_name": "NuCarePharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076194", "marketing_category": "ANDA", "marketing_start_date": "20030301", "listing_expiration_date": "20261231"}