lisinopril and hydrochlorothiazide (68645-557)

Drug Facts

Product Profile

Brand Name lisinopril and hydrochlorothiazide

Generic Name lisinopril and hydrochlorothiazide

Labeler legacy pharmaceutical packaging, llc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 12.5 mg/1, lisinopril 20 mg/1

Manufacturer

Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-557

Product ID 68645-557_4c4ae743-258c-e380-e063-6394a90af48a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA077912

Listing Expiration 2027-12-31

Marketing Start 2006-04-10

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 68645557

Hyphenated Format 68645-557

Supplemental Identifiers

RxCUI

197885 197886 197887

UPC

0368645556543 0368645557540 0368645558547

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

12.5 mg/1
20 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE (68645-557-54)

source: ndc

Packages (1)

68645-557-54 30 TABLET in 1 BOTTLE (68645-557-54)

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": "4c4ae743-258c-e380-e063-6394a90af48a", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368645556543", "0368645557540", "0368645558547"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["6d729ec5-7311-4534-9999-9d6fa4f3ba2f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-557-54)", "package_ndc": "68645-557-54", "marketing_start_date": "20060410"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68645-557_4c4ae743-258c-e380-e063-6394a90af48a", "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": "68645-557", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "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": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20060410", "listing_expiration_date": "20271231"}