Lamotrigine

Product NDC
50090-5567
11-digit product format
500905567
Labeler code
50090
Product ID
50090-5567_b50f93ad-56e0-42a0-a8d8-31dd7acddedf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lamotrigine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077633
Marketing category
ANDA
Marketing start
2009-01-27
Marketing end
0000-00-00
Substance
LAMOTRIGINE
Active strength
25 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
14a9502b-3d70-0496-a7e1-b16edaa005b8Product name520250423
16d731ed-ff3e-e9a1-3e3e-1ef6b6be40a0Product name720250401
e29d8e8b-4bc8-ebaf-f18e-e35287b19d6aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-5567-0Lamotrigine33 in 1 CARTONTABLET3310
50090-5567-0Lamotrigine1 in 1 BLISTER PACKTABLET110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-5567LAMOTRIGINE TABLET [A-S MEDICATION SOLUTIONS]10Legacy NDC, 2 package rows20211118_d210bf04-094a-4713-a940-72fed91a5f71.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
282401lamoTRIgine 25 MG Oral TabletPSNd210bf04-094a-4713-a940-72fed91a5f7110
282401lamotrigine 25 MG Oral TabletSCDd210bf04-094a-4713-a940-72fed91a5f7110

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5567-05009055670033 BLISTER PACK in 1 CARTON (50090-5567-0) > 1 TABLET in 1 BLISTER PACK33 blister pack2021-06-220000-00-00NoNoCurrent