lisinopril and hydrochlorothiazide (68180-520)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler lupin pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1

Manufacturer

Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-520

Product ID 68180-520_4035482a-7e09-464f-ae01-a8a75fc3c4c1

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA077912

Listing Expiration 2026-12-31

Marketing Start 2006-10-04

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 68180520

Hyphenated Format 68180-520

Supplemental Identifiers

RxCUI

197885 197886 197887

UPC

0368180519010 0368180518013 0368180520016

UNII

0J48LPH2TH E7199S1YWR

NUI

N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager

true

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 ANDA077912 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
20 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (68180-520-01)
500 TABLET in 1 BOTTLE (68180-520-02)
5000 TABLET in 1 POUCH (68180-520-30)

source: ndc

Packages (3)

68180-520-01 100 TABLET in 1 BOTTLE (68180-520-01) 68180-520-02 500 TABLET in 1 BOTTLE (68180-520-02) 68180-520-30 5000 TABLET in 1 POUCH (68180-520-30)

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": "4035482a-7e09-464f-ae01-a8a75fc3c4c1", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368180519010", "0368180518013", "0368180520016"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["515f735c-5dba-43d9-8a58-97a319cafd56"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-520-01)", "package_ndc": "68180-520-01", "marketing_start_date": "20061004"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68180-520-02)", "package_ndc": "68180-520-02", "marketing_start_date": "20061004"}, {"sample": false, "description": "5000 TABLET in 1 POUCH (68180-520-30)", "package_ndc": "68180-520-30", "marketing_start_date": "20061004"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68180-520_4035482a-7e09-464f-ae01-a8a75fc3c4c1", "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": "68180-520", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Lupin Pharmaceuticals, Inc.", "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": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20061004", "listing_expiration_date": "20261231"}