Bisoprolol Fumarate and Hydrochlorothiazide
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
- Bisoprolol Fumarate and Hydrochlorothiazide
- Generic name
- BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 35ed3030-a9b3-4e4e-99cd-6d5c31ad22fa
- SPL ID
- 9d6e36f0-a9e4-4b66-997a-fd5f8e4e1cf7
- Version
- 1
- Effective date
- 2022-11-07
- Source export date
- 2026-11-06
- 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/2026-11-06/968b7138703f8100b14008bced2b2a4531f4fab250b207279e9c05eb19608f40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:14:53
| 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 | 215666 | derived:openfda.application_number |
| application number | ANDA215666 | openfda.application_number | |
| brand name | Bisoprolol Fumarate and Hydrochlorothiazide | openfda.brand_name | |
| generic name | BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1760-1 | openfda.package_ndc |
| ndc | package | 70771-1761-5 | openfda.package_ndc |
| ndc | package | 70771-1761-1 | openfda.package_ndc |
| ndc | package | 70771-1762-1 | openfda.package_ndc |
| ndc | package | 70771-1760-5 | openfda.package_ndc |
| ndc | package | 70771-1761-3 | openfda.package_ndc |
| ndc | package | 70771-1760-3 | openfda.package_ndc |
| ndc | package | 70771-1762-3 | openfda.package_ndc |
| ndc | package | 70771-1762-5 | openfda.package_ndc |
| ndc | product | 70771-1761 | openfda.product_ndc |
| ndc | product | 70771-1760 | openfda.product_ndc |
| ndc | product | 70771-1762 | openfda.product_ndc |
| ndc11 | package | 70771176103 | derived:openfda.package_ndc |
| ndc11 | package | 70771176203 | derived:openfda.package_ndc |
| ndc11 | package | 70771176105 | derived:openfda.package_ndc |
| ndc11 | package | 70771176001 | derived:openfda.package_ndc |
| ndc11 | package | 70771176201 | derived:openfda.package_ndc |
| ndc11 | package | 70771176003 | derived:openfda.package_ndc |
| ndc11 | package | 70771176005 | derived:openfda.package_ndc |
| ndc11 | package | 70771176101 | derived:openfda.package_ndc |
| ndc11 | package | 70771176205 | derived:openfda.package_ndc |
| rxcui | 854908 | openfda.rxcui | |
| rxcui | 854919 | openfda.rxcui | |
| rxcui | 854916 | openfda.rxcui | |
| spl id | 9d6e36f0-a9e4-4b66-997a-fd5f8e4e1cf7 | id | |
| spl set id | 35ed3030-a9b3-4e4e-99cd-6d5c31ad22fa | set_id | |
| unii | UR59KN573L | openfda.unii | |
| unii | 0J48LPH2TH | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.