Nadolol
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
- Nadolol
- Generic name
- NADOLOL
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 29433c5a-51c6-4fb9-9174-1b1c616c9e57
- SPL ID
- af4aa709-b3ff-49c4-91d5-353a99d46696
- Version
- 7
- Effective date
- 2024-12-05
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:15:45
| 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 | 207761 | derived:openfda.application_number |
| application number | ANDA207761 | openfda.application_number | |
| brand name | Nadolol | openfda.brand_name | |
| generic name | NADOLOL | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1091-2 | openfda.package_ndc |
| ndc | package | 70771-1090-1 | openfda.package_ndc |
| ndc | package | 70771-1091-0 | openfda.package_ndc |
| ndc | package | 70771-1090-2 | openfda.package_ndc |
| ndc | package | 70771-1090-0 | openfda.package_ndc |
| ndc | package | 70771-1089-9 | openfda.package_ndc |
| ndc | package | 70771-1089-4 | openfda.package_ndc |
| ndc | package | 70771-1089-2 | openfda.package_ndc |
| ndc | package | 70771-1089-1 | openfda.package_ndc |
| ndc | package | 70771-1090-9 | openfda.package_ndc |
| ndc | package | 70771-1091-1 | openfda.package_ndc |
| ndc | package | 70771-1091-9 | openfda.package_ndc |
| ndc | package | 70771-1090-4 | openfda.package_ndc |
| ndc | package | 70771-1091-4 | openfda.package_ndc |
| ndc | package | 70771-1089-0 | openfda.package_ndc |
| ndc | product | 70771-1091 | openfda.product_ndc |
| ndc | product | 70771-1089 | openfda.product_ndc |
| ndc | product | 70771-1090 | openfda.product_ndc |
| ndc11 | package | 70771109002 | derived:openfda.package_ndc |
| ndc11 | package | 70771109104 | derived:openfda.package_ndc |
| ndc11 | package | 70771108901 | derived:openfda.package_ndc |
| ndc11 | package | 70771108902 | derived:openfda.package_ndc |
| ndc11 | package | 70771109009 | derived:openfda.package_ndc |
| ndc11 | package | 70771108900 | derived:openfda.package_ndc |
| ndc11 | package | 70771108904 | derived:openfda.package_ndc |
| ndc11 | package | 70771109102 | derived:openfda.package_ndc |
| ndc11 | package | 70771109000 | derived:openfda.package_ndc |
| ndc11 | package | 70771109100 | derived:openfda.package_ndc |
| ndc11 | package | 70771109101 | derived:openfda.package_ndc |
| ndc11 | package | 70771109001 | derived:openfda.package_ndc |
| ndc11 | package | 70771108909 | derived:openfda.package_ndc |
| ndc11 | package | 70771109109 | derived:openfda.package_ndc |
| ndc11 | package | 70771109004 | derived:openfda.package_ndc |
| rxcui | 198007 | openfda.rxcui | |
| rxcui | 198006 | openfda.rxcui |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.