NDC 51672-4130-01 - 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
- 51672-4130
- Requested NDC
- 51672-4130-01
- Package NDCs from labels
- 51672-4130-6, 51672-4130-4, 51672-4130-1, 51672-4130-3, 51672-4130-0, 51672-4130-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2026-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lamotrigine | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2026-06-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - REMEDYREPACK INC. | REMEDYREPACK INC. | 2025-06-27 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - Preferred Pharmaeuticals Inc. | Preferred Pharmaeuticals Inc. | 2024-06-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - ST. MARY'S MEDICAL PARK PHARMACY | ST. MARY'S MEDICAL PARK PHARMACY | 2022-07-27 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - A-S Medication Solutions | A-S Medication Solutions | 2018-07-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - A-S Medication Solutions | A-S Medication Solutions | 2018-06-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2015-01-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Lamotrigine - Rebel Distributors Corp | Rebel Distributors Corp | 2010-09-30 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4130-0 | Lamotrigine | 10 in 1 BLISTER PACK | TABLET | 10 | 21 | |
| 51672-4130-0 | Lamotrigine | 10 in 1 CARTON | TABLET | 10 | 21 | |
| 51672-4130-1 | Lamotrigine | 100 in 1 BOTTLE | TABLET | 100 | 21 | |
| 51672-4130-3 | Lamotrigine | 1000 in 1 BOTTLE | TABLET | 1000 | 21 | |
| 51672-4130-4 | Lamotrigine | 60 in 1 BOTTLE | TABLET | 60 | 21 | |
| 51672-4130-6 | Lamotrigine | 30 in 1 BOTTLE | TABLET | 30 | 21 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-4130 | LAMOTRIGINE TABLET [TARO PHARMACEUTICALS U.S.A., INC.] | 15 | Current NDC, Legacy NDC, 6 package rows | 20230517_b829f9b2-f0ac-408a-a6f4-18b72150227d.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-4130-1 | EA - Each | 51672-4130 | b1138f13-a1a8-4495-a8a5-2c4d49568df5 | 1 | 2012-07-24 |
| 51672-4130-3 | EA - Each | 51672-4130 | 33c9112c-59c4-4d89-834e-19e4d2ec8233 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 Kit | LAMOTRIGINE | OWP Pharmaceuticals, Inc. | 474fb321-575c-4b97-9dbe-080061652ee4 | 2026-03-27 | Boxed warning, Warnings, Adverse reactions | 282401 198427 U3H27498KS |
| SUBVENITE | LAMOTRIGINE | OWP Pharmaceuticals, Inc. | 7ad18b68-ba16-4810-9c3e-27fa970454e8 | 2026-03-27 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Alembic Pharmaceuticals Limited | 03610cdf-7eaa-445c-a441-ff17be5a7c68 | 2026-03-26 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Rising Pharma Holdings, Inc. | f54690b3-bcbb-4d94-95b9-b7591af00117 | 2026-03-26 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Dynamic Brain | ARGENTUM NITRICUM, CUPRUM ACETICUM, GINKGO BILOBA, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, PHOSPHORICUM ACIDUM, THIAMINUM HYDROCHLORICUM, CEREBRUM SUIS, AMBRA GRISEA, PICRICUM ACIDUM, AGNUS CASTUS, ALUMINA, ANACARDIUM ORIENTALE, BARYTA CARBONICA, CICUTA VIROSA, CONIUM MACULATUM, HELLEBORUS NIGER, PLUMBUM METALLICUM, SELENIUM METALLICUM, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 60a1e44b-3f91-41de-82c2-4648fb800dcd | 2026-03-19 | Warnings | LMI26O6933 |
| Lamotrigine | LAMOTRIGINE | REMEDYREPACK INC. | 260dc37d-6e64-4688-82dc-10a1a428af17 | 2026-03-19 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Aurobindo Pharma Limited | e08920c2-04a3-4fb5-acc5-0af3140f82e9 | 2026-03-18 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Leader Advanced Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Cardinal Health | 5c5d6c13-9b51-48f0-8627-b60b0f707fd3 | 2026-03-12 | Warnings | FZ989GH94E |
| Skin Irritations and Itch Relief | AGARICUS MUSCARIUS, ALUMINA, ANAGALLIS ARVENSIS, ANTIMONIUM TARTARICUM, APIS MELLIFICA, ARSENICUM ALBUM, ARSENICUM IODATUM, BOVISTA, CAUSTICUM, DOLICHOS PRURIENS, FAGOPYRUM ESCULENTUM, GRAPHITES, KALI MURIATICUM, MURIATICUM ACIDUM, OLEANDER, PETROLEUM, PIX LIQUIDA, RADIUM BROMATUM (12X, 30X, 1LM), RHUS TOX, SELENIUM METALLICUM, SULPHUR AND URTICA URENS. | King Bio Inc. | d139d2f1-0369-4963-9f3d-c4cc0f1ea2dd | 2026-03-10 | Warnings | LMI26O6933 |
| Lamotrigine | LAMOTRIGINE | Torrent Pharmaceuticals Limited | 52df02a7-83da-4b20-9951-69790237dc24 | 2026-03-04 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Total Body Detox | ALUMINA, BRYONIA, CALCAREA IODATA, CANTHARIS, CARDUUS BENEDICTUS, CARDUUS MAR, CHELIDONIUM MAJ, CINCHONA OFFICINALIS, CYNARA SCOLYMUS, DIOSCOREA VILLOSA, HEPAR SULPHURIS CALCAREUM, IRIS VERSICOLOR, JUNIPERUS COMMUNIS, KALI IODATUM, MERCURIUS CORROSIVUS, MERCURIUS VIVUS, NATRUM CARBONICUM, NUX VOMICA, PLUMBUM METALLICUM, PTELEA TRIFOLIATA, RICINUS COMMUNIS, ROBINIA PSEUDOACACIA, SERUM ANGUILLAE, SOLIDAGO VIRGAUREA, SULPHUR, SULPHURICUM ACIDUM AND TARAXACUM OFFICINALE. | King Bio Inc. | c803733e-b5e2-46f2-bdfe-b239f38d9312 | 2026-03-04 | Warnings | LMI26O6933 |
| Lamotrigine | LAMOTRIGINE | Alembic Pharmaceuticals Inc. | df34faa4-829e-413a-a230-cbec604eead9 | 2026-03-02 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | American Health Packaging | 6034a8b8-9e80-43ca-b84f-ea82f788268c | 2026-03-02 | Boxed warning, Warnings, Adverse reactions | 198428 198429 U3H27498KS |
| lamotrigine | LAMOTRIGINE | Alembic Pharmaceuticals Inc. | 05cba628-b12c-44d8-89a8-3522fe417cc1 | 2026-02-26 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Alembic Pharmaceuticals Inc. | 4bd7193f-a81a-4909-90c2-7f324fc6ddfd | 2026-02-23 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| MERC CORR | ALUMINA, BRYONIA, COLOCYNTHIS, CHINA OFF, LYCOPODIUM, THUJA OCC, NUX VOM | BM Private Limited | 3b29d70d-f291-dad2-e063-6294a90a07f5 | 2026-02-12 | Warnings | LMI26O6933 |
| GoodSense Eye Drops Advanced Relief Moisturizer | DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Sportpharm LLC | 8d58dcbb-72a0-41f0-9eeb-613072a6d7ae | 2026-02-06 | Warnings | FZ989GH94E |
| MINIDROPS | LUBRICANT EYE DROPS | Optics Laboratory, Inc | c13c5f91-50df-471c-a7c9-1747a2ac1250 | 2026-02-03 | Warnings | FZ989GH94E |
| lamotrigine | LAMOTRIGINE EXTENDED-RELEASE | Camber Pharmaceuticals Inc | e45bd69f-3580-ff15-e053-2a95a90a4615 | 2026-02-02 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Glenmark Pharmaceuticals Inc., USA | 50fcf452-2d21-493e-a1dd-0c6ea9ac6184 | 2026-01-29 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.