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
- 8c0eeefc-ef5b-49f4-8411-ddbae312ed05
- SPL ID
- ba40713a-2f22-4276-a664-355e7442cda4
- Version
- 3
- Effective date
- 2025-09-15
- 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 01:44:51
| 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 | 203934 | derived:openfda.application_number |
| application number | ANDA203934 | 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 | 70771-1862-5 | openfda.package_ndc |
| ndc | package | 70771-1862-4 | openfda.package_ndc |
| ndc | package | 70771-1918-1 | openfda.package_ndc |
| ndc | package | 70771-1862-9 | openfda.package_ndc |
| ndc | package | 70771-1861-2 | openfda.package_ndc |
| ndc | package | 70771-1916-1 | openfda.package_ndc |
| ndc | package | 70771-1917-6 | openfda.package_ndc |
| ndc | package | 70771-1862-2 | openfda.package_ndc |
| ndc | package | 70771-1861-5 | openfda.package_ndc |
| ndc | package | 70771-1917-1 | openfda.package_ndc |
| ndc | package | 70771-1918-6 | openfda.package_ndc |
| ndc | package | 70771-1916-6 | openfda.package_ndc |
| ndc | package | 70771-1861-9 | openfda.package_ndc |
| ndc | product | 70771-1917 | openfda.product_ndc |
| ndc | product | 70771-1862 | openfda.product_ndc |
| ndc | product | 70771-1916 | openfda.product_ndc |
| ndc | product | 70771-1918 | openfda.product_ndc |
| ndc | product | 70771-1861 | openfda.product_ndc |
| ndc11 | package | 70771186202 | derived:openfda.package_ndc |
| ndc11 | package | 70771191601 | derived:openfda.package_ndc |
| ndc11 | package | 70771191706 | derived:openfda.package_ndc |
| ndc11 | package | 70771186205 | derived:openfda.package_ndc |
| ndc11 | package | 70771191606 | derived:openfda.package_ndc |
| ndc11 | package | 70771186102 | derived:openfda.package_ndc |
| ndc11 | package | 70771191801 | derived:openfda.package_ndc |
| ndc11 | package | 70771186209 | derived:openfda.package_ndc |
| ndc11 | package | 70771186204 | derived:openfda.package_ndc |
| ndc11 | package | 70771191701 | derived:openfda.package_ndc |
| ndc11 | package | 70771186109 | derived:openfda.package_ndc |
| ndc11 | package | 70771186105 | derived:openfda.package_ndc |
| ndc11 | package | 70771191806 | derived:openfda.package_ndc |
| rxcui | 2634747 | openfda.rxcui | |
| rxcui | 1806380 | openfda.rxcui | |
| rxcui | 2634743 | openfda.rxcui | |
| rxcui | 2634751 | openfda.rxcui |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.