Tamsulosin Hydrochloride
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
- Tamsulosin Hydrochloride
- Generic name
- TAMSULOSIN HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 276c7e26-f86a-46b9-b626-ceef76b729a4
- SPL ID
- b05d1829-8334-4145-b49d-6074624bc499
- Version
- 9
- Effective date
- 2024-08-12
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:31:08
| 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 | 078225 | derived:openfda.application_number |
| application number | ANDA078225 | openfda.application_number | |
| brand name | Tamsulosin Hydrochloride | openfda.brand_name | |
| generic name | TAMSULOSIN HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-695-16 | openfda.package_ndc |
| ndc | package | 65841-695-14 | openfda.package_ndc |
| ndc | package | 65841-695-77 | openfda.package_ndc |
| ndc | package | 65841-695-05 | openfda.package_ndc |
| ndc | package | 65841-695-10 | openfda.package_ndc |
| ndc | package | 65841-695-06 | openfda.package_ndc |
| ndc | package | 65841-695-01 | openfda.package_ndc |
| ndc | product | 65841-695 | openfda.product_ndc |
| ndc11 | package | 65841069505 | derived:openfda.package_ndc |
| ndc11 | package | 65841069514 | derived:openfda.package_ndc |
| ndc11 | package | 65841069506 | derived:openfda.package_ndc |
| ndc11 | package | 65841069510 | derived:openfda.package_ndc |
| ndc11 | package | 65841069516 | derived:openfda.package_ndc |
| ndc11 | package | 65841069577 | derived:openfda.package_ndc |
| ndc11 | package | 65841069501 | derived:openfda.package_ndc |
| rxcui | 863669 | openfda.rxcui | |
| spl id | b05d1829-8334-4145-b49d-6074624bc499 | id | |
| spl set id | 276c7e26-f86a-46b9-b626-ceef76b729a4 | set_id | |
| unii | 11SV1951MR | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.