Lamotrigine
- Product NDC
- 51407-061
- 11-digit product format
- 514070061
- Labeler code
- 51407
- Product ID
- 51407-061_cb0a656d-1a32-36d8-e053-2995a90aa666
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA206382
- Marketing category
- ANDA
- Marketing start
- 2016-06-17
- Marketing end
- 0000-00-00
- Substance
- LAMOTRIGINE
- Active strength
- 50 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-061-30 | 51407006130 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (51407-061-30) | 2018-04-12 | 0000-00-00 | No | No | Current |