Lamotrigine
- Product NDC
- 70771-1517
- 11-digit product format
- 707711517
- Labeler code
- 70771
- Product ID
- 70771-1517_c2007dd5-98b7-47e2-8354-7ce432174a48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lamotirigine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA207763
- Marketing category
- ANDA
- Marketing start
- 2020-05-14
- 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
- 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 | 850087, 850091, 900156, 900164, 1098608, 1146690 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1517-2 | Lamotrigine | 10 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 10 | | 5 |
| 70771-1517-3 | Lamotrigine | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 5 |
| 70771-1517-4 | Lamotrigine | 10 in 1 CARTON | TABLET, EXTENDED RELEASE | 10 | | 5 |
| 70771-1517-5 | Lamotrigine | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | | 5 |
| 70771-1517-9 | Lamotrigine | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1517 | LAMOTRIGINE (LAMOTIRIGINE) TABLET, EXTENDED RELEASE [ZYDUS LIFESCIENCES LIMITED] | 5 | Current NDC, Legacy NDC, 5 package rows | 20241204_ecb7a528-699f-4e51-9887-dee60456da2f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1517-2 | 70771151702 | 10 in 1 BLISTER PACK | | | | | | Historical |
| 70771-1517-3 | 70771151703 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1517-3) | | 2020-05-14 | 0000-00-00 | No | No | Current |
| 70771-1517-4 | 70771151704 | 10 BLISTER PACK in 1 CARTON (70771-1517-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70771-1517-2) | 10 blister pack | 2020-05-14 | 0000-00-00 | No | No | Current |
| 70771-1517-5 | 70771151705 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1517-5) | | 2020-05-14 | 0000-00-00 | No | No | Current |
| 70771-1517-9 | 70771151709 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1517-9) | | 2020-05-14 | 0000-00-00 | No | No | Current |