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
- MSN LABORATORIES PRIVATE LIMITED
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 0ae4e2d1-305d-4045-95da-cfe7c2d8b435
- SPL ID
- 421cfdea-11a0-4fd7-8b8f-79711f1e5f89
- Version
- 2
- Effective date
- 2022-04-21
- Source export date
- 2026-10-12
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:40:32
| 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 | 204921 | derived:openfda.application_number |
| application number | ANDA204921 | openfda.application_number | |
| brand name | lacosamide | openfda.brand_name | |
| generic name | LACOSAMIDE | openfda.generic_name | |
| manufacturer name | MSN LABORATORIES PRIVATE LIMITED | openfda.manufacturer_name | |
| ndc | package | 69539-028-05 | openfda.package_ndc |
| ndc | package | 69539-025-05 | openfda.package_ndc |
| ndc | package | 69539-028-60 | openfda.package_ndc |
| ndc | package | 69539-025-60 | openfda.package_ndc |
| ndc | package | 69539-027-05 | openfda.package_ndc |
| ndc | package | 69539-027-60 | openfda.package_ndc |
| ndc | package | 69539-026-05 | openfda.package_ndc |
| ndc | package | 69539-026-60 | openfda.package_ndc |
| ndc | product | 69539-027 | openfda.product_ndc |
| ndc | product | 69539-028 | openfda.product_ndc |
| ndc | product | 69539-026 | openfda.product_ndc |
| ndc | product | 69539-025 | openfda.product_ndc |
| ndc11 | package | 69539002605 | derived:openfda.package_ndc |
| ndc11 | package | 69539002805 | derived:openfda.package_ndc |
| ndc11 | package | 69539002505 | derived:openfda.package_ndc |
| ndc11 | package | 69539002560 | derived:openfda.package_ndc |
| ndc11 | package | 69539002760 | derived:openfda.package_ndc |
| ndc11 | package | 69539002860 | derived:openfda.package_ndc |
| ndc11 | package | 69539002660 | derived:openfda.package_ndc |
| ndc11 | package | 69539002705 | derived:openfda.package_ndc |
| rxcui | 809996 | openfda.rxcui | |
| rxcui | 810000 | openfda.rxcui | |
| rxcui | 809987 | openfda.rxcui | |
| rxcui | 809992 | openfda.rxcui | |
| spl id | 421cfdea-11a0-4fd7-8b8f-79711f1e5f89 | id | |
| spl set id | 0ae4e2d1-305d-4045-95da-cfe7c2d8b435 | set_id | |
| unii | 563KS2PQY5 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.