LACOSAMIDE
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
- LACOSAMIDE
- Generic name
- LACOSAMIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 3bc84c70-bc1d-4a72-bbe7-86f32cd646d0
- SPL ID
- 96b87696-5bfd-4306-b00e-c66e7b93f071
- Version
- 2
- Effective date
- 2023-10-03
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:54:29
| Harmonized routes |
|---|
| INTRAVENOUS |
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 | 209465 | derived:openfda.application_number |
| application number | ANDA209465 | openfda.application_number | |
| brand name | LACOSAMIDE | openfda.brand_name | |
| generic name | LACOSAMIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1682-6 | openfda.package_ndc |
| ndc | package | 70771-1682-1 | openfda.package_ndc |
| ndc | product | 70771-1682 | openfda.product_ndc |
| ndc11 | package | 70771168201 | derived:openfda.package_ndc |
| ndc11 | package | 70771168206 | derived:openfda.package_ndc |
| rxcui | 809974 | openfda.rxcui | |
| spl id | 96b87696-5bfd-4306-b00e-c66e7b93f071 | id | |
| spl set id | 3bc84c70-bc1d-4a72-bbe7-86f32cd646d0 | set_id | |
| unii | 563KS2PQY5 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.