Lamotrigine

Product NDC
64679-274
11-digit product format
646790274
Labeler code
64679
Product ID
64679-274_b7778fde-0a8a-0857-e053-2995a90a2240
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lamotrigine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Wockhardt USA LLC.
Application
ANDA202498
Marketing category
ANDA
Marketing start
2012-11-29
Marketing end
0000-00-00
Substance
LAMOTRIGINE
Active strength
50 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
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
64679-274-01EA - Each64679-274124a01a1-40d2-4f88-b1ac-34cbe9c5d9cd12013-02-13
64679-274-02EA - Each64679-274434dd468-4e4a-433d-8aec-627fb7e157d212013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64679-274LAMOTRIGINE TABLET, EXTENDED RELEASE [WOCKHARDT USA LLC.]5Legacy NDC20201228_0e9b23d9-0813-4fb5-848d-776453f361f7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
64679-274-016467902740130 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-274-01) 2012-11-290000-00-00NoNoCurrent
64679-274-0264679027402500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-274-02) 2012-11-290000-00-00NoNoCurrent
64679-274-036467902740310 BLISTER PACK in 1 CARTON (64679-274-03) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (64679-274-04) 10 blister pack2012-11-290000-00-00NoNoCurrent