FDA.reportPublic FDA data

BZP hydrochloride 20 MG Oral Tablet [Lotensin]

RxCUI
898692
RxNorm name
BZP hydrochloride 20 MG Oral Tablet [Lotensin]
Display name
BZP hydrochloride 20 MG Oral Tablet [Lotensin]
Full name
BZP hydrochloride 20 MG Oral Tablet [Lotensin]
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:51

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LotensinBENAZEPRIL HYDROCHLORIDEValidus Pharmaceuticals LLC2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e2025-09-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898692

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
2abb091b-a53e-46b0-9b84-e5ee8f2bdd8eLotensin 20 MG Oral Tablet [PSN] · benazepril hydrochloride 20 MG Oral Tablet [Lotensin] [SBD] · BZP hydrochloride 20 MG Oral Tablet [Lotensin] [SY] · Lotensin 20 MG Oral Tablet [SY]410These highlights do not include all the information needed to use LOTENSIN ® safely and effectively. See full prescribing information for use LOTENSIN ® . LOTENSIN ® (benazepril hydrochloride, USP) tablets, for oral use Initial U.S. Approval: 199120250930
f2da9586-8baa-4852-8669-80dade6363cfLotensin 20 MG Oral Tablet [PSN] · benazepril hydrochloride 20 MG Oral Tablet [Lotensin] [SBD] · BZP hydrochloride 20 MG Oral Tablet [Lotensin] [SY] · Lotensin 20 MG Oral Tablet [SY]43Lotensin20120301