lisinopril and hydrochlorothiazide (68788-9808)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler preferred pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1

Manufacturer

Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-9808

Product ID 68788-9808_bdd60a26-e62a-4941-a89f-48c7c870c9b1

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA077912

Listing Expiration 2026-12-31

Marketing Start 2012-04-23

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 687889808

Hyphenated Format 68788-9808

Supplemental Identifiers

RxCUI

197885 197886 197887

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 ANDA077912 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
20 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (68788-9808-1)
30 TABLET in 1 BOTTLE (68788-9808-3)
60 TABLET in 1 BOTTLE (68788-9808-6)
90 TABLET in 1 BOTTLE (68788-9808-9)

source: ndc

Packages (4)

68788-9808-1 100 TABLET in 1 BOTTLE (68788-9808-1) 68788-9808-3 30 TABLET in 1 BOTTLE (68788-9808-3) 68788-9808-6 60 TABLET in 1 BOTTLE (68788-9808-6) 68788-9808-9 90 TABLET in 1 BOTTLE (68788-9808-9)

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": "bdd60a26-e62a-4941-a89f-48c7c870c9b1", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["5aa18b0b-4688-493a-a5ae-cb056ea6c0e3"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-9808-1)", "package_ndc": "68788-9808-1", "marketing_start_date": "20120423"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-9808-3)", "package_ndc": "68788-9808-3", "marketing_start_date": "20120423"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-9808-6)", "package_ndc": "68788-9808-6", "marketing_start_date": "20120423"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-9808-9)", "package_ndc": "68788-9808-9", "marketing_start_date": "20120423"}], "brand_name": "LISINOPRIL AND HYDROCHLOROTHIAZIDE", "product_id": "68788-9808_bdd60a26-e62a-4941-a89f-48c7c870c9b1", "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": "68788-9808", "generic_name": "LISINOPRIL AND HYDROCHLOROTHIAZIDE", "labeler_name": "Preferred 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": "20120423", "listing_expiration_date": "20261231"}