Gabapentin
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
- Gabapentin
- Generic name
- GABAPENTIN
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b033c169-4943-4ad9-ace0-7e4a1f0dc100
- SPL ID
- e9f9a5e6-0454-4601-90e4-b170bb325eb6
- Version
- 8
- Effective date
- 2024-11-30
- 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 01:40:41
| 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 | 078926 | derived:openfda.application_number |
| application number | ANDA078926 | openfda.application_number | |
| brand name | Gabapentin | openfda.brand_name | |
| generic name | GABAPENTIN | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-706-77 | openfda.package_ndc |
| ndc | package | 65841-706-01 | openfda.package_ndc |
| ndc | package | 65841-705-10 | openfda.package_ndc |
| ndc | package | 65841-705-01 | openfda.package_ndc |
| ndc | package | 65841-706-10 | openfda.package_ndc |
| ndc | package | 65841-706-05 | openfda.package_ndc |
| ndc | package | 65841-705-05 | openfda.package_ndc |
| ndc | product | 65841-705 | openfda.product_ndc |
| ndc | product | 65841-706 | openfda.product_ndc |
| ndc11 | package | 65841070601 | derived:openfda.package_ndc |
| ndc11 | package | 65841070501 | derived:openfda.package_ndc |
| ndc11 | package | 65841070610 | derived:openfda.package_ndc |
| ndc11 | package | 65841070605 | derived:openfda.package_ndc |
| ndc11 | package | 65841070505 | derived:openfda.package_ndc |
| ndc11 | package | 65841070677 | derived:openfda.package_ndc |
| ndc11 | package | 65841070510 | derived:openfda.package_ndc |
| rxcui | 310433 | openfda.rxcui | |
| rxcui | 310434 | openfda.rxcui | |
| spl id | e9f9a5e6-0454-4601-90e4-b170bb325eb6 | id | |
| spl set id | b033c169-4943-4ad9-ace0-7e4a1f0dc100 | set_id | |
| unii | 6CW7F3G59X | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.