Lamotrigine
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Lamotrigine
- Generic name
- LAMOTIRIGINE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ecb7a528-699f-4e51-9887-dee60456da2f
- SPL ID
- c2007dd5-98b7-47e2-8354-7ce432174a48
- Version
- 5
- Effective date
- 2024-11-30
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:54:37
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 207763 | derived:openfda.application_number |
| application number | ANDA207763 | openfda.application_number | |
| brand name | Lamotrigine | openfda.brand_name | |
| generic name | LAMOTIRIGINE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1517-3 | openfda.package_ndc |
| ndc | package | 70771-1516-5 | openfda.package_ndc |
| ndc | package | 70771-1515-4 | openfda.package_ndc |
| ndc | package | 70771-1518-9 | openfda.package_ndc |
| ndc | package | 70771-1514-2 | openfda.package_ndc |
| ndc | package | 70771-1519-4 | openfda.package_ndc |
| ndc | package | 70771-1514-5 | openfda.package_ndc |
| ndc | package | 70771-1517-4 | openfda.package_ndc |
| ndc | package | 70771-1514-4 | openfda.package_ndc |
| ndc | package | 70771-1518-4 | openfda.package_ndc |
| ndc | package | 70771-1519-5 | openfda.package_ndc |
| ndc | package | 70771-1515-2 | openfda.package_ndc |
| ndc | package | 70771-1514-3 | openfda.package_ndc |
| ndc | package | 70771-1519-9 | openfda.package_ndc |
| ndc | package | 70771-1517-9 | openfda.package_ndc |
| ndc | package | 70771-1518-2 | openfda.package_ndc |
| ndc | package | 70771-1519-2 | openfda.package_ndc |
| ndc | package | 70771-1515-5 | openfda.package_ndc |
| ndc | package | 70771-1516-9 | openfda.package_ndc |
| ndc | package | 70771-1514-9 | openfda.package_ndc |
| ndc | package | 70771-1516-2 | openfda.package_ndc |
| ndc | package | 70771-1516-3 | openfda.package_ndc |
| ndc | package | 70771-1515-3 | openfda.package_ndc |
| ndc | package | 70771-1517-2 | openfda.package_ndc |
| ndc | package | 70771-1519-3 | openfda.package_ndc |
| ndc | package | 70771-1518-3 | openfda.package_ndc |
| ndc | package | 70771-1517-5 | openfda.package_ndc |
| ndc | package | 70771-1515-9 | openfda.package_ndc |
| ndc | package | 70771-1516-4 | openfda.package_ndc |
| ndc | package | 70771-1518-5 | openfda.package_ndc |
| ndc | product | 70771-1518 | openfda.product_ndc |
| ndc | product | 70771-1517 | openfda.product_ndc |
| ndc | product | 70771-1516 | openfda.product_ndc |
| ndc | product | 70771-1514 | openfda.product_ndc |
| ndc | product | 70771-1515 | openfda.product_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.