Lisinopril

Product NDC
53808-0703
11-digit product format
538080703
Labeler code
53808
Product ID
53808-0703_27c6283e-54e1-4ae0-a07a-dc71d92a6de2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LISINOPRIL
Dosage form
TABLET
Route
ORAL
Labeler
State of Florida DOH Central Pharmacy
Application
ANDA076059
Marketing category
ANDA
Marketing start
2009-07-01
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53808-0703-12019-10-21C16284748780-1956f9ecf-bf34-621f-e053-dbdaa90a74adONCE-DAILY Lisinopril Tablets USP Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53808-0703-1Lisinopril30 in 1 BLISTER PACKTABLET302

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53808-0703LISINOPRIL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2Legacy NDC, 1 package rows20100324_7076fa36-403c-4a2f-8d45-10c0b36b65fc.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
314077lisinopril 20 MG Oral TabletPSN7076fa36-403c-4a2f-8d45-10c0b36b65fc2
314077lisinopril 20 MG Oral TabletSCD7076fa36-403c-4a2f-8d45-10c0b36b65fc2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
53808-0703-15380807030130 in 1 BLISTER PACKHistorical