NDC 55111-221-79 - 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
- 55111-221
- Requested NDC
- 55111-221-79
- Package NDCs from labels
- 55111-221-30, 55111-221-60, 55111-221-01, 55111-221-05, 55111-221-79, 55111-221-78
- Manufacturer
- Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited FTO-3
- Effective date
- 2024-12-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lamotrigine - Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited FTO-3 | Dr.Reddy's Laboratories Limited | Dr.Reddy's Laboratories Limited FTO-3 | 2024-12-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-221-01 | Lamotrigine | 100 in 1 BOTTLE | TABLET | 100 | 11 | |
| 55111-221-05 | Lamotrigine | 500 in 1 BOTTLE | TABLET | 500 | 11 | |
| 55111-221-30 | Lamotrigine | 30 in 1 BOTTLE | TABLET | 30 | 11 | |
| 55111-221-60 | Lamotrigine | 60 in 1 BOTTLE | TABLET | 60 | 11 | |
| 55111-221-78 | Lamotrigine | 10 in 1 CARTON | TABLET | 10 | 11 | |
| 55111-221-79 | Lamotrigine | 10 in 1 BLISTER PACK | TABLET | 10 | 11 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-221-01 | EA - Each | 55111-221 | a62522b4-7c51-4592-9529-3e11ad0420f8 | 1 | 2012-07-24 |
| 55111-221-05 | EA - Each | 55111-221 | f0476f37-8011-483e-891a-fee540fe3263 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LAMOTRIGINE | ACTIVE INGREDIENT | U3H27498KS | LAMOTRIGINE TABLET [DR.REDDY'S LABORATORIES LIMITED] | 9 | |
| Lamotrigine | ACTIVE MOIETY | U3H27498KS | LAMOTRIGINE TABLET [DR.REDDY'S LABORATORIES LIMITED] | 9 |
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 | 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 |
| lamotrigine | LAMOTRIGINE EXTENDED-RELEASE | Yiling Pharmaceutical, Inc. | f7de11a5-5357-4753-b1ac-b15123b50028 | 2025-12-29 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | A-S Medication Solutions | 84277e2c-370c-4510-92bc-ef33a4a0f508 | 2025-12-05 | Boxed warning, Warnings, Adverse reactions | 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Amneal Pharmaceuticals of New York LLC | 9e5c2d76-47a6-4a57-b23c-2398b307380c | 2025-12-04 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Ajanta Pharma USA Inc. | 9dfb5f87-0150-4c26-a89f-34f1ab389500 | 2025-11-26 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Dr.Reddy's Laboratories Limited | a69542ea-5b6f-15c1-9e7a-90ac839971d3 | 2025-11-21 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | NorthStar Rx LLC | 9ab07d6b-ae4a-a310-5572-b266676cd29e | 2025-11-20 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Advagen Pharma Limited | 4ca9d713-ab63-48bf-9386-29301a842e60 | 2025-11-19 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Zydus Pharmaceuticals USA Inc. | e849033b-a3bc-408e-88de-7cd1d2660949 | 2025-11-14 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 8f8f53e3-fe31-e7b5-e053-2995a90a710d | 2025-11-14 | Warnings | 3OWL53L36A |
| QR PAIN | ANALGESIC | MARYHELENE ENTERPRISES INC | 9984a510-30be-4013-e053-2995a90a841e | 2025-11-14 | Warnings | 3OWL53L36A |
| Lamotrigine | LAMOTRIGINE | Zydus Pharmaceuticals USA Inc. | eb436371-d188-4803-a864-07b90c357e57 | 2025-11-12 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Mannitol | MANNITOL | ProPharma Distribution | 430669d7-9ad1-9a04-e063-6394a90ababb | 2025-11-07 | Warnings, Adverse reactions | 3OWL53L36A |
| Sorbitol-Mannitol | SORBITOL AND MANNITOL | ICU Medical Inc. | 5b44e248-4b7b-4777-954a-921c7b309944 | 2025-10-30 | Warnings, Adverse reactions | 3OWL53L36A |
| Mannitol | MANNITOL | ICU Medical Inc. | ba7bf864-8a4d-4262-8fd1-00174fa2f9d1 | 2025-10-24 | Warnings, Adverse reactions | 3OWL53L36A |
| LAMICTAL | LAMOTRIGINE | GlaxoSmithKline LLC | d7e3572d-56fe-4727-2bb4-013ccca22678 | 2025-10-10 | Boxed warning, Warnings, Adverse reactions | 282401 198428 198427 198429 U3H27498KS |
| LAMICTAL XR | LAMOTRIGINE | GlaxoSmithKline LLC | 3e2c9a35-6a39-41d7-ad84-3c0bb8894b09 | 2025-10-10 | Boxed warning, Warnings, Adverse reactions | U3H27498KS |
| Lamotrigine | LAMOTRIGINE | Zydus Lifesciences Limited | 0f2f7421-56d4-45d0-9d2d-dc1edaede039 | 2025-10-04 | 282401 198428 198427 198429 U3H27498KS | |
| Lamotrigine | LAMOTRIGINE | Bryant Ranch Prepack | 8e1e4fa8-881c-4618-88f6-018ab15db44d | 2025-09-18 | Boxed warning, Warnings, Adverse reactions | 198428 U3H27498KS |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.