Lamotrigine
- Product NDC
- 68788-9526
- 11-digit product format
- 687889526
- Labeler code
- 68788
- Product ID
- 68788-9526_ab977789-d551-4c81-b6b3-c32a7aebad3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA079132
- Marketing category
- ANDA
- Marketing start
- 2014-01-20
- 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