Lamotrigine
- Product NDC
- 55154-8137
- 11-digit product format
- 551548137
- Labeler code
- 55154
- Product ID
- 55154-8137_59e7f9bf-09d7-4f1f-8693-bdc920f96ab8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077633
- Marketing category
- ANDA
- Marketing start
- 2009-01-27
- Marketing end
- 0000-00-00
- Substance
- LAMOTRIGINE
- Active strength
- 25 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-8137-0 | 55154813700 | 10 BLISTER PACK in 1 BAG (55154-8137-0) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2009-01-27 | 0000-00-00 | No | No | Current |