budesonide
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
- budesonide
- Generic name
- BUDESONIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d645a346-c99b-4de7-9bca-69e73266d6b4
- SPL ID
- bfde9c2e-2ff5-4258-91bc-78a48b228d14
- Version
- 8
- Effective date
- 2025-02-12
- Source export date
- 2026-10-30
- 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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:27:14
| 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 | 206134 | derived:openfda.application_number |
| application number | ANDA206134 | openfda.application_number | |
| brand name | budesonide | openfda.brand_name | |
| generic name | BUDESONIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1075-3 | openfda.package_ndc |
| ndc | package | 70771-1075-1 | openfda.package_ndc |
| ndc | package | 70771-1075-9 | openfda.package_ndc |
| ndc | package | 70771-1075-4 | openfda.package_ndc |
| ndc | package | 70771-1075-0 | openfda.package_ndc |
| ndc | package | 70771-1075-5 | openfda.package_ndc |
| ndc | product | 70771-1075 | openfda.product_ndc |
| ndc11 | package | 70771107504 | derived:openfda.package_ndc |
| ndc11 | package | 70771107509 | derived:openfda.package_ndc |
| ndc11 | package | 70771107500 | derived:openfda.package_ndc |
| ndc11 | package | 70771107501 | derived:openfda.package_ndc |
| ndc11 | package | 70771107505 | derived:openfda.package_ndc |
| ndc11 | package | 70771107503 | derived:openfda.package_ndc |
| rxcui | 1244214 | openfda.rxcui | |
| spl id | bfde9c2e-2ff5-4258-91bc-78a48b228d14 | id | |
| spl set id | d645a346-c99b-4de7-9bca-69e73266d6b4 | set_id | |
| unii | Q3OKS62Q6X | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.