Labetalol 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
- Labetalol Hydrochloride
- Generic name
- LABETALOL HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- a3c0cc1e-1c01-4009-afdc-d35a66546aec
- SPL ID
- 2be8d068-1830-4767-9e97-8d774d9a6001
- Version
- 6
- Effective date
- 2024-11-30
- 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 01:44:10
| 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 | 207743 | derived:openfda.application_number |
| application number | ANDA207743 | openfda.application_number | |
| brand name | Labetalol Hydrochloride | openfda.brand_name | |
| generic name | LABETALOL HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1163-1 | openfda.package_ndc |
| ndc | package | 70771-1164-3 | openfda.package_ndc |
| ndc | package | 70771-1163-5 | openfda.package_ndc |
| ndc | package | 70771-1165-5 | openfda.package_ndc |
| ndc | package | 70771-1164-9 | openfda.package_ndc |
| ndc | package | 70771-1163-9 | openfda.package_ndc |
| ndc | package | 70771-1164-5 | openfda.package_ndc |
| ndc | package | 70771-1164-1 | openfda.package_ndc |
| ndc | package | 70771-1163-3 | openfda.package_ndc |
| ndc | package | 70771-1165-9 | openfda.package_ndc |
| ndc | package | 70771-1165-1 | openfda.package_ndc |
| ndc | package | 70771-1165-3 | openfda.package_ndc |
| ndc | product | 70771-1165 | openfda.product_ndc |
| ndc | product | 70771-1164 | openfda.product_ndc |
| ndc | product | 70771-1163 | openfda.product_ndc |
| ndc11 | package | 70771116305 | derived:openfda.package_ndc |
| ndc11 | package | 70771116401 | derived:openfda.package_ndc |
| ndc11 | package | 70771116405 | derived:openfda.package_ndc |
| ndc11 | package | 70771116409 | derived:openfda.package_ndc |
| ndc11 | package | 70771116503 | derived:openfda.package_ndc |
| ndc11 | package | 70771116301 | derived:openfda.package_ndc |
| ndc11 | package | 70771116403 | derived:openfda.package_ndc |
| ndc11 | package | 70771116509 | derived:openfda.package_ndc |
| ndc11 | package | 70771116303 | derived:openfda.package_ndc |
| ndc11 | package | 70771116501 | derived:openfda.package_ndc |
| ndc11 | package | 70771116505 | derived:openfda.package_ndc |
| ndc11 | package | 70771116309 | derived:openfda.package_ndc |
| rxcui | 896766 | openfda.rxcui | |
| rxcui | 896758 | openfda.rxcui | |
| rxcui | 896762 | openfda.rxcui | |
| spl id | 2be8d068-1830-4767-9e97-8d774d9a6001 | id | |
| spl set id | a3c0cc1e-1c01-4009-afdc-d35a66546aec | set_id | |
| unii | 1GEV3BAW9J | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.