Lamotrigine

Product NDC
64679-272
11-digit product format
646790272
Labeler code
64679
Product ID
64679-272_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
200 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
64679-272-01EA - Each64679-2723d4bdbca-b2a4-4d1f-b190-30028af68c3a12013-02-13
64679-272-02EA - Each64679-272ba66b3b3-6f4d-47ed-92dc-6122ced662f012013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64679-272LAMOTRIGINE 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
64679-272-016467902720130 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-272-01) 2012-11-290000-00-00NoNoCurrent
64679-272-0264679027202500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64679-272-02) 2012-11-290000-00-00NoNoCurrent
64679-272-046467902720410 BLISTER PACK in 1 CARTON (64679-272-04) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (64679-272-03) 10 blister pack2012-11-290000-00-00NoNoCurrent