Duloxetine
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
- Duloxetine
- Generic name
- DULOXETINE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f36b414e-ace4-4f04-a80f-75bb25db430d
- SPL ID
- 22968719-7127-4aab-b4c4-4497de16ca23
- Version
- 7
- Effective date
- 2024-11-28
- Source export date
- 2026-11-06
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:18:26
| 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 | 090739 | derived:openfda.application_number |
| application number | ANDA090739 | openfda.application_number | |
| brand name | Duloxetine | openfda.brand_name | |
| generic name | DULOXETINE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-800-16 | openfda.package_ndc |
| ndc | package | 65841-799-14 | openfda.package_ndc |
| ndc | package | 65841-801-10 | openfda.package_ndc |
| ndc | package | 65841-800-06 | openfda.package_ndc |
| ndc | package | 65841-799-16 | openfda.package_ndc |
| ndc | package | 65841-801-16 | openfda.package_ndc |
| ndc | package | 65841-800-10 | openfda.package_ndc |
| ndc | package | 65841-801-06 | openfda.package_ndc |
| ndc | package | 65841-799-06 | openfda.package_ndc |
| ndc | product | 65841-800 | openfda.product_ndc |
| ndc | product | 65841-801 | openfda.product_ndc |
| ndc | product | 65841-799 | openfda.product_ndc |
| ndc11 | package | 65841080106 | derived:openfda.package_ndc |
| ndc11 | package | 65841080010 | derived:openfda.package_ndc |
| ndc11 | package | 65841080110 | derived:openfda.package_ndc |
| ndc11 | package | 65841079906 | derived:openfda.package_ndc |
| ndc11 | package | 65841080116 | derived:openfda.package_ndc |
| ndc11 | package | 65841080006 | derived:openfda.package_ndc |
| ndc11 | package | 65841080016 | derived:openfda.package_ndc |
| ndc11 | package | 65841079916 | derived:openfda.package_ndc |
| ndc11 | package | 65841079914 | derived:openfda.package_ndc |
| rxcui | 596926 | openfda.rxcui | |
| rxcui | 596930 | openfda.rxcui | |
| rxcui | 596934 | openfda.rxcui | |
| spl id | 22968719-7127-4aab-b4c4-4497de16ca23 | id | |
| spl set id | f36b414e-ace4-4f04-a80f-75bb25db430d | set_id | |
| unii | 9044SC542W | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.