Lamotrigine ER
- Product NDC
- 72189-467
- 11-digit product format
- 721890467
- Labeler code
- 72189
- Product ID
- 72189-467_2c4ddaed-38a0-7cd7-e063-6294a90a148f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotrigine ER
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA207763
- Marketing category
- ANDA
- Marketing start
- 2023-05-03
- Substance
- LAMOTRIGINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lamotrigine ER
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LAMOTRIGINE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3H27498KS |
| Rxcui | 900156 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-467-30 | Lamotrigine ER | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-467 | LAMOTRIGINE ER TABLET, EXTENDED RELEASE [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_faccacb7-65f1-cb00-e053-6394a90a9fcb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-467-30 | 72189046730 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-467-30) | 2023-05-03 | No | No | Historical |