Lamotrigine

Product NDC
0615-7546
11-digit product format
006157546
Labeler code
0615
Product ID
0615-7546_6bf9a99a-7d36-4e31-b6b5-5ea65b5e942e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lamotrigine
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA076388
Marketing category
ANDA
Marketing start
2008-07-22
Marketing end
0000-00-00
Substance
LAMOTRIGINE
Active strength
150 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7546-392021-07-07C16284748780-19d75b9d1-03e4-f424-e053-dadaa90a57ce8e2fc056-755f-447a-98d6-351879729e13
0615-7546-392020-01-31C16284748780-19d75b9d1-03e4-f424-e053-dadaa90a57ce8e2fc056-755f-447a-98d6-351879729e13