candesartan cilexetil 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
- candesartan cilexetil and hydrochlorothiazide
- Generic name
- CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- cb328bc1-5738-4620-b2b3-442e98388a86
- SPL ID
- 2b38d778-d732-4a7b-bb34-b426a14e10bc
- Version
- 5
- Effective date
- 2024-11-11
- Source export date
- 2026-09-28
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:41:51
| 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 | 203466 | derived:openfda.application_number |
| application number | ANDA203466 | openfda.application_number | |
| brand name | candesartan cilexetil and hydrochlorothiazide | openfda.brand_name | |
| generic name | CANDESARTAN CILEXETIL AND HYDROCHLOROTHIAZIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1327-2 | openfda.package_ndc |
| ndc | package | 70771-1325-0 | openfda.package_ndc |
| ndc | package | 70771-1325-2 | openfda.package_ndc |
| ndc | package | 70771-1326-2 | openfda.package_ndc |
| ndc | package | 70771-1327-9 | openfda.package_ndc |
| ndc | package | 70771-1326-9 | openfda.package_ndc |
| ndc | package | 70771-1327-3 | openfda.package_ndc |
| ndc | package | 70771-1325-3 | openfda.package_ndc |
| ndc | package | 70771-1326-1 | openfda.package_ndc |
| ndc | package | 70771-1327-4 | openfda.package_ndc |
| ndc | package | 70771-1327-1 | openfda.package_ndc |
| ndc | package | 70771-1325-9 | openfda.package_ndc |
| ndc | package | 70771-1326-0 | openfda.package_ndc |
| ndc | package | 70771-1325-4 | openfda.package_ndc |
| ndc | package | 70771-1326-4 | openfda.package_ndc |
| ndc | package | 70771-1327-0 | openfda.package_ndc |
| ndc | package | 70771-1326-3 | openfda.package_ndc |
| ndc | package | 70771-1325-1 | openfda.package_ndc |
| ndc | product | 70771-1325 | openfda.product_ndc |
| ndc | product | 70771-1327 | openfda.product_ndc |
| ndc | product | 70771-1326 | openfda.product_ndc |
| ndc11 | package | 70771132709 | derived:openfda.package_ndc |
| ndc11 | package | 70771132601 | derived:openfda.package_ndc |
| ndc11 | package | 70771132702 | derived:openfda.package_ndc |
| ndc11 | package | 70771132504 | derived:openfda.package_ndc |
| ndc11 | package | 70771132501 | derived:openfda.package_ndc |
| ndc11 | package | 70771132603 | derived:openfda.package_ndc |
| ndc11 | package | 70771132500 | derived:openfda.package_ndc |
| ndc11 | package | 70771132703 | derived:openfda.package_ndc |
| ndc11 | package | 70771132602 | derived:openfda.package_ndc |
| ndc11 | package | 70771132600 | derived:openfda.package_ndc |
| ndc11 | package | 70771132700 | derived:openfda.package_ndc |
| ndc11 | package | 70771132604 | derived:openfda.package_ndc |
| ndc11 | package | 70771132701 | derived:openfda.package_ndc |
| ndc11 | package | 70771132509 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.