Lisinopril

Product NDC
21695-345
11-digit product format
216950345
Labeler code
21695
Product ID
21695-345_81210afd-6505-4d38-ab83-e276ee4ce144
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp
Application
ANDA077321
Marketing category
ANDA
Marketing start
2008-02-01
Marketing end
0000-00-00
Substance
LISINOPRIL
Active strength
3 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
21695-345-302019-09-24C16284748780-1934fe258-473d-48b1-e053-8cdaa90a720aLISINOPRIL TABLETS USP - PACKAGE LABELS
21695-345-902019-09-24C16284748780-1934fe258-473d-48b1-e053-8cdaa90a720aLISINOPRIL TABLETS USP - PACKAGE LABELS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-345-30Lisinopril30 in 1 BOTTLETABLET302
21695-345-90Lisinopril90 in 1 BOTTLETABLET902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-345-30EA - Each21695-3451e6504cc-4d7f-4aa6-b851-e42052def42512012-07-24
21695-345-90EA - Each21695-3456c7f7845-12e2-4fee-a6fa-09948b8942c512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LISINOPRILACTIVE INGREDIENTE7199S1YWRLISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
LISINOPRILACTIVE MOIETYE7199S1YWRLISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
ANHYDROUS DIBASIC CALCIUM PHOSPHATEINACTIVE INGREDIENTL11K75P92JLISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30LISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
MANNITOLINACTIVE INGREDIENT3OWL53L36ALISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4LISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJLISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-345LISINOPRIL TABLET [REBEL DISTRIBUTORS CORP]2Legacy NDC, 2 package rows20111208_9b73c97f-b898-471f-be8a-96324a3e3b86.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311353lisinopril 2.5 MG Oral TabletPSN9b73c97f-b898-471f-be8a-96324a3e3b862
311353lisinopril 2.5 MG Oral TabletSCD9b73c97f-b898-471f-be8a-96324a3e3b862

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
21695-345-302169503453030 in 1 BOTTLEHistorical
21695-345-902169503459090 in 1 BOTTLEHistorical