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 Extended-Release | LAMOTRIGINE | Par Health USA, LLC | d5ec4d58-c669-4ab4-ba62-b71007536854 | 2026-01-21 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Preferred Pharmaceuticals Inc. | 634dbe6c-4874-4d54-aa25-be02d3341f16 | 2026-01-14 | Boxed warning, Warnings, Adverse reactions | 198427 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | AvKARE | a63e19c0-a093-e896-e053-2a95a90a7ccd | 2026-01-14 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | LMI26O6933 |
| Lamotrigine | LAMOTRIGINE | NuCare Pharmaceuticals, Inc. | 47fd2592-2fc6-9787-e063-6394a90a8f01 | 2026-01-09 | Boxed warning, Warnings, Adverse reactions | ANDA078525 198427 U3H27498KS |
| Metex 6013 | METEX | Professional Complementary Health Formulas | 78371ca3-50a6-46f0-8ea6-7de57c516375 | 2026-01-08 | Warnings | LMI26O6933 |
| H-Clenz Drops 2026 | H-CLENZ DROPS | Professional Complementary Health Formulas | 5dd76d36-e3db-472a-82f8-30643e49eaf7 | 2026-01-08 | Warnings | LMI26O6933 |
| Alumina Combination 9204 | ALUMINA COMBINATION | Professional Complementary Health Formulas | 312cac13-2009-4b8f-a09b-9be2d2801df5 | 2026-01-08 | Warnings | LMI26O6933 |
| Alopecia Formula 2139 | ALOPECIA FORMULA | Professional Complementary Health Formulas | ce0eaf67-a435-4167-b9ce-c0ff1f8a9dc2 | 2026-01-08 | Warnings | LMI26O6933 |
| Colic Drops 2155 | COLIC DROPS | Professional Complementary Health Formulas | 17b9e92f-f4ed-48b4-ab02-8b7cba0a2027 | 2026-01-08 | Warnings | LMI26O6933 |
| Colostat | RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALOE, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, NUX VOMICA, PODOPHYLLUM PELTATUM | Energique, Inc. | 3ddbed50-7ca9-493c-ba94-321c2afef60e | 2026-01-06 | Warnings | LMI26O6933 |
| Lamotrigine | LAMOTRIGINE | Quallent Pharmaceuticals Health LLC | 7977c87f-b459-486a-9edc-0a2071c46f4c | 2026-01-03 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Northwind Health Company, LLC | 03fd8413-df56-50ab-e063-6394a90a6950 | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 198427 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Northwind Health Company, LLC | db5f7ee5-9bd9-1819-e053-2a95a90a91df | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 282401 U3H27498KS |
| LAMOTRIGINE | LAMOTRIGINE | Northwind Health Company, LLC | f7587283-781b-e111-e053-6394a90ad4cc | 2026-01-01 | Boxed warning, Warnings, Adverse reactions | 282401 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Northstar Rx LLC. | aabc64fe-1f17-4140-81f2-7d4506db6c8b | 2025-12-31 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| CVS Advanced Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE | CVS Pharmacy, Inc. | f74a2fca-902c-f68a-e053-6394a90abb88 | 2025-12-30 | Warnings | FZ989GH94E |
| Good Sense Artificial Tears | POLYVINYL ALCOHOL, POVIDONE | Geiss, Destin & Dunn, Inc. | 9b243301-2e4b-5706-e053-2995a90a9b90 | 2025-12-30 | Warnings | FZ989GH94E |
| GoodSense Eye Drops Advanced Relief Moisturizer | DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Geiss, Derstin & Dunn, Inc. | 9b34de99-13df-201a-e053-2a95a90ae559 | 2025-12-30 | Warnings | FZ989GH94E |
| Discount Drug Mart Eye Drops Advanced Relief | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE | Discount Drug Mart, Inc. | f75c2f84-a28c-5807-e053-6294a90a2295 | 2025-12-30 | Warnings | FZ989GH94E |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.