Dexamethasone
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
- Dexamethasone
- Generic name
- DEXAMETHASONE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 522a1a49-5540-4245-a15f-e3cdc0a97a5e
- SPL ID
- ebc1bd42-82a5-40dc-ab21-b8d5252518b3
- Version
- 2
- Effective date
- 2024-03-30
- Source export date
- 2026-11-06
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:43:12
| 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 | 216282 | derived:openfda.application_number |
| application number | ANDA216282 | openfda.application_number | |
| brand name | Dexamethasone | openfda.brand_name | |
| generic name | DEXAMETHASONE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1699-1 | openfda.package_ndc |
| ndc | package | 70771-1707-1 | openfda.package_ndc |
| ndc | package | 70771-1704-1 | openfda.package_ndc |
| ndc | package | 70771-1705-1 | openfda.package_ndc |
| ndc | package | 70771-1700-1 | openfda.package_ndc |
| ndc | product | 70771-1699 | openfda.product_ndc |
| ndc | product | 70771-1705 | openfda.product_ndc |
| ndc | product | 70771-1700 | openfda.product_ndc |
| ndc | product | 70771-1704 | openfda.product_ndc |
| ndc | product | 70771-1707 | openfda.product_ndc |
| ndc11 | package | 70771170701 | derived:openfda.package_ndc |
| ndc11 | package | 70771170501 | derived:openfda.package_ndc |
| ndc11 | package | 70771170001 | derived:openfda.package_ndc |
| ndc11 | package | 70771169901 | derived:openfda.package_ndc |
| ndc11 | package | 70771170401 | derived:openfda.package_ndc |
| rxcui | 343033 | openfda.rxcui | |
| rxcui | 197577 | openfda.rxcui | |
| rxcui | 197582 | openfda.rxcui | |
| rxcui | 197580 | openfda.rxcui | |
| rxcui | 197583 | openfda.rxcui | |
| spl id | ebc1bd42-82a5-40dc-ab21-b8d5252518b3 | id | |
| spl set id | 522a1a49-5540-4245-a15f-e3cdc0a97a5e | set_id | |
| unii | 7S5I7G3JQL | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.