Eletriptan hydrobromide
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
- Eletriptan hydrobromide
- Generic name
- ELETRIPTAN HYDROBROMIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 481ae7d4-9e57-424a-9d07-2920954b6ddc
- SPL ID
- b0459347-b3de-466e-b386-85665dd294c9
- Version
- 7
- Effective date
- 2024-11-28
- Source export date
- 2026-10-30
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:56:25
| 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 | 206409 | derived:openfda.application_number |
| application number | ANDA206409 | openfda.application_number | |
| brand name | Eletriptan hydrobromide | openfda.brand_name | |
| generic name | ELETRIPTAN HYDROBROMIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1107-6 | openfda.package_ndc |
| ndc | package | 70771-1107-2 | openfda.package_ndc |
| ndc | package | 70771-1107-4 | openfda.package_ndc |
| ndc | package | 70771-1108-2 | openfda.package_ndc |
| ndc | package | 70771-1107-3 | openfda.package_ndc |
| ndc | package | 70771-1108-5 | openfda.package_ndc |
| ndc | package | 70771-1108-3 | openfda.package_ndc |
| ndc | package | 70771-1108-6 | openfda.package_ndc |
| ndc | package | 70771-1107-0 | openfda.package_ndc |
| ndc | package | 70771-1108-4 | openfda.package_ndc |
| ndc | product | 70771-1107 | openfda.product_ndc |
| ndc | product | 70771-1108 | openfda.product_ndc |
| ndc11 | package | 70771110702 | derived:openfda.package_ndc |
| ndc11 | package | 70771110806 | derived:openfda.package_ndc |
| ndc11 | package | 70771110700 | derived:openfda.package_ndc |
| ndc11 | package | 70771110706 | derived:openfda.package_ndc |
| ndc11 | package | 70771110802 | derived:openfda.package_ndc |
| ndc11 | package | 70771110804 | derived:openfda.package_ndc |
| ndc11 | package | 70771110703 | derived:openfda.package_ndc |
| ndc11 | package | 70771110805 | derived:openfda.package_ndc |
| ndc11 | package | 70771110704 | derived:openfda.package_ndc |
| ndc11 | package | 70771110803 | derived:openfda.package_ndc |
| rxcui | 359493 | openfda.rxcui | |
| rxcui | 359494 | openfda.rxcui | |
| spl id | b0459347-b3de-466e-b386-85665dd294c9 | id | |
| spl set id | 481ae7d4-9e57-424a-9d07-2920954b6ddc | set_id | |
| unii | M41W832TA3 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.