Lamotrigine
- Product NDC
- 70518-2108
- 11-digit product format
- 705182108
- Labeler code
- 70518
- Product ID
- 70518-2108_9722efae-e215-e61a-e053-2995a90a3335
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078525
- Marketing category
- ANDA
- Marketing start
- 2019-05-23
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2108 | LAMOTRIGINE TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250306_2c1a246f-6830-498e-ab67-1f037420737a.zip |