Topiramate
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
- Topiramate
- Generic name
- TOPIRAMATE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9a943af0-1c6d-43c2-830a-f303baa16124
- SPL ID
- 709dd70b-24e1-435f-8373-02e6dd538b2c
- Version
- 6
- Effective date
- 2023-11-08
- Source export date
- 2026-10-12
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:37:05
| 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 | 207382 | derived:openfda.application_number |
| application number | ANDA207382 | openfda.application_number | |
| brand name | Topiramate | openfda.brand_name | |
| generic name | TOPIRAMATE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1858-8 | openfda.package_ndc |
| ndc | package | 70771-1315-5 | openfda.package_ndc |
| ndc | package | 70771-1317-9 | openfda.package_ndc |
| ndc | package | 70771-1858-3 | openfda.package_ndc |
| ndc | package | 70771-1316-3 | openfda.package_ndc |
| ndc | package | 70771-1316-5 | openfda.package_ndc |
| ndc | package | 70771-1316-4 | openfda.package_ndc |
| ndc | package | 70771-1315-4 | openfda.package_ndc |
| ndc | package | 70771-1858-5 | openfda.package_ndc |
| ndc | package | 70771-1316-2 | openfda.package_ndc |
| ndc | package | 70771-1858-2 | openfda.package_ndc |
| ndc | package | 70771-1317-1 | openfda.package_ndc |
| ndc | package | 70771-1317-2 | openfda.package_ndc |
| ndc | package | 70771-1315-2 | openfda.package_ndc |
| ndc | package | 70771-1315-3 | openfda.package_ndc |
| ndc | package | 70771-1858-1 | openfda.package_ndc |
| ndc | package | 70771-1316-9 | openfda.package_ndc |
| ndc | package | 70771-1316-1 | openfda.package_ndc |
| ndc | package | 70771-1317-3 | openfda.package_ndc |
| ndc | package | 70771-1317-4 | openfda.package_ndc |
| ndc | package | 70771-1315-9 | openfda.package_ndc |
| ndc | package | 70771-1315-1 | openfda.package_ndc |
| ndc | package | 70771-1317-5 | openfda.package_ndc |
| ndc | product | 70771-1315 | openfda.product_ndc |
| ndc | product | 70771-1858 | openfda.product_ndc |
| ndc | product | 70771-1317 | openfda.product_ndc |
| ndc | product | 70771-1316 | openfda.product_ndc |
| ndc11 | package | 70771131504 | derived:openfda.package_ndc |
| ndc11 | package | 70771131503 | derived:openfda.package_ndc |
| ndc11 | package | 70771131502 | derived:openfda.package_ndc |
| ndc11 | package | 70771185802 | derived:openfda.package_ndc |
| ndc11 | package | 70771131603 | derived:openfda.package_ndc |
| ndc11 | package | 70771131505 | derived:openfda.package_ndc |
| ndc11 | package | 70771185803 | derived:openfda.package_ndc |
| ndc11 | package | 70771185801 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.