LISINOPRIL

Product NDC
10544-239
11-digit product format
105440239
Labeler code
10544
Product ID
10544-239_ba16b206-e57f-4593-997b-4856244c5400
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LISINOPRIL
Dosage form
TABLET
Route
ORAL
Labeler
Blenheim Pharmacal, Inc.
Application
ANDA077321
Marketing category
ANDA
Marketing start
2009-12-16
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
20 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f8f05a6d-f74b-4e9e-ab1c-374d3b4fb820Product name120230703
f65307a7-3644-0a09-cdfd-94aae8d3b53eProduct name320210902
1bdb87cf-9b1f-6a51-5eb7-d182aaffaa3dProduct name220170719

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10544-239-30LISINOPRIL30 in 1 BOTTLETABLET301
10544-239-60LISINOPRIL60 in 1 BOTTLETABLET601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10544-239LISINOPRIL TABLET [BLENHEIM PHARMACAL, INC.]1Legacy NDC, 2 package rows20100908_a1c30704-69a4-47fa-b948-9fbc38f2ef85.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
314077lisinopril 20 MG Oral TabletPSNa1c30704-69a4-47fa-b948-9fbc38f2ef851
314077lisinopril 20 MG Oral TabletSCDa1c30704-69a4-47fa-b948-9fbc38f2ef851

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10544-239-301054402393030 in 1 BOTTLEHistorical
10544-239-601054402396060 in 1 BOTTLEHistorical