FDA.reportPublic FDA data

Lamotrigine

Product NDC
51672-4133
11-digit product format
516724133
Labeler code
51672
Product ID
51672-4133_44812d3c-0fc0-67dd-e063-6394a90a9d70
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lamotrigine
Dosage form
TABLET
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc.
Application
ANDA078525
Marketing category
ANDA
Marketing start
2009-01-27
Substance
LAMOTRIGINE
Active strength
200 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Lamotrigine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LAMOTRIGINE200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU3H27498KS
Rxcui198427, 198428, 198429, 282401

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-4133-0Lamotrigine10 in 1 BLISTER PACKTABLET1021
51672-4133-0Lamotrigine10 in 1 CARTONTABLET1021
51672-4133-1Lamotrigine100 in 1 BOTTLETABLET10021
51672-4133-2Lamotrigine500 in 1 BOTTLETABLET50021
51672-4133-3Lamotrigine1000 in 1 BOTTLETABLET100021
51672-4133-4Lamotrigine60 in 1 BOTTLETABLET6021
51672-4133-6Lamotrigine30 in 1 BOTTLETABLET3021

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-4133LAMOTRIGINE TABLET [TARO PHARMACEUTICALS U.S.A., INC.]15Current NDC, Legacy NDC, 7 package rows20230517_b829f9b2-f0ac-408a-a6f4-18b72150227d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198427lamoTRIgine 100 MG Oral TabletPSN7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
198428lamoTRIgine 150 MG Oral TabletPSN7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
198429lamoTRIgine 200 MG Oral TabletPSN7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
282401lamoTRIgine 25 MG Oral TabletPSN7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
198427lamotrigine 100 MG Oral TabletSCD7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
198428lamotrigine 150 MG Oral TabletSCD7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
198429lamotrigine 200 MG Oral TabletSCD7332e0ea-fbd0-43fb-8d1e-f7068504c61d1
282401lamotrigine 25 MG Oral TabletSCD7332e0ea-fbd0-43fb-8d1e-f7068504c61d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51672-4133-05167241330010 BLISTER PACK in 1 CARTON (51672-4133-0) / 10 TABLET in 1 BLISTER PACK10 blister pack2009-01-270000-00-00NoNoCurrent
51672-4133-151672413301100 TABLET in 1 BOTTLE (51672-4133-1) 100 tablet2009-01-270000-00-00NoNoCurrent
51672-4133-251672413302500 TABLET in 1 BOTTLE (51672-4133-2) 500 tablet2022-10-250000-00-00NoNoCurrent
51672-4133-3516724133031000 TABLET in 1 BOTTLE (51672-4133-3) 1000 tablet2009-01-270000-00-00NoNoCurrent
51672-4133-45167241330460 TABLET in 1 BOTTLE (51672-4133-4) 60 tablet2009-01-270000-00-00NoNoCurrent
51672-4133-65167241330630 TABLET in 1 BOTTLE (51672-4133-6) 30 tablet2009-01-270000-00-00NoNoCurrent