LAMOTRIGINE

Product NDC
50090-2466
11-digit product format
500902466
Labeler code
50090
Product ID
50090-2466_476978aa-74cc-45f0-937e-a3dc4dcfda82
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lamotrigine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077783
Marketing category
ANDA
Marketing start
2010-11-01
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
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2466-0EA - Each50090-2466c1414527-6d1d-4d33-99b5-7e6747aa443812019-03-12