NDC 70518-2108-2 - Lamotrigine
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 70518-2108
- Requested NDC
- 70518-2108-2
- Package NDCs from labels
- 70518-2108-0, 70518-2108-2, 70518-2108-1
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2025-06-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lamotrigine - REMEDYREPACK INC. | REMEDYREPACK INC. | 2025-06-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-2108 | LAMOTRIGINE TABLET [REMEDYREPACK INC.] | 9 | Legacy NDC | 20250306_2c1a246f-6830-498e-ab67-1f037420737a.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| lamotrigine | LAMOTRIGINE CHEWABLE DISPERSIBLE | Alembic Pharmaceuticals Limited | ae6522d4-d824-44aa-afe0-70cdcbd845af | 2023-01-17 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Ascend Laboratories, LLC | 70cd448a-2921-4c69-bdf2-5a6ce883bd07 | 2022-12-09 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | ScieGen Pharmaceuticals, Inc. | de700ac1-4048-467e-abb1-238953261a97 | 2022-11-03 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Proficient Rx LP | 52273d60-3f27-4846-bf40-014ebcf09417 | 2022-05-02 | Boxed warning, Warnings, Adverse reactions | 198427 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Proficient Rx LP | b94ae2e4-e276-40c1-bc25-da980194fc99 | 2022-04-01 | Boxed warning, Warnings, Adverse reactions | 282401 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Asclemed USA, Inc. | 8ac9dc83-edb2-4ae5-8064-40f113fd3aab | 2020-10-14 | Boxed warning, Warnings, Adverse reactions | 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Dr.Reddy's Laboratories Limited | e1a0da17-d67c-e44f-bd42-33c4009e4cdd | 2018-12-10 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Amneal Pharmaceuticals of New York LLC | 380bddae-5b31-4965-96de-97711d859d11 | 2016-02-02 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.