LAMOTRIGINE
- Product NDC
- 50090-3171
- 11-digit product format
- 500903171
- Labeler code
- 50090
- Product ID
- 50090-3171_a32a144c-5f74-4dc2-9e3a-ee6f565cd281
- 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
- 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
- 2020-12-31
- 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 |
|---|
| 50090-3171-0 | 50090317100 | 60 TABLET in 1 BOTTLE (50090-3171-0) | 60 tablet | 2017-10-13 | 0000-00-00 | No | No | Current |
| 50090-3171-1 | 50090317101 | 180 TABLET in 1 BOTTLE, PLASTIC (50090-3171-1) | 180 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |