lisinopril and hydrochlorothiazide (43063-468)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler pd-rx pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1

Manufacturer

PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-468

Product ID 43063-468_47d238b7-b5d5-0e63-e063-6294a90a8027

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA077912

Listing Expiration 2027-12-31

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 43063468

Hyphenated Format 43063-468

Supplemental Identifiers

RxCUI

197887

UPC

0343063468302

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

30 TABLET in 1 BOTTLE, PLASTIC (43063-468-30)
90 TABLET in 1 BOTTLE, PLASTIC (43063-468-90)

source: ndc

Packages (2)

43063-468-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-468-30) 43063-468-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-468-90)

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": "47d238b7-b5d5-0e63-e063-6294a90a8027", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0343063468302"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197887"], "spl_set_id": ["00f67e1a-6999-4295-9c9f-fcb1ce9711b8"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-468-30)", "package_ndc": "43063-468-30", "marketing_start_date": "20130913"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-468-90)", "package_ndc": "43063-468-90", "marketing_start_date": "20130913"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "43063-468_47d238b7-b5d5-0e63-e063-6294a90a8027", "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": "43063-468", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "PD-Rx 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": "20271231"}