estradiol
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
- estradiol
- Generic name
- ESTRADIOL
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 2f2030c2-f72e-4142-9cff-540bc8fbf8a1
- SPL ID
- 7287c5b3-80de-4eab-9905-f597a4fbaf34
- Version
- 1
- Effective date
- 2023-04-21
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:44:02
| Harmonized routes |
|---|
| TRANSDERMAL |
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 | 204379 | derived:openfda.application_number |
| application number | ANDA204379 | openfda.application_number | |
| brand name | estradiol | openfda.brand_name | |
| generic name | ESTRADIOL | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1400-1 | openfda.package_ndc |
| ndc | package | 70771-1400-4 | openfda.package_ndc |
| ndc | product | 70771-1400 | openfda.product_ndc |
| ndc11 | package | 70771140001 | derived:openfda.package_ndc |
| ndc11 | package | 70771140004 | derived:openfda.package_ndc |
| rxcui | 476545 | openfda.rxcui | |
| spl id | 7287c5b3-80de-4eab-9905-f597a4fbaf34 | id | |
| spl set id | 2f2030c2-f72e-4142-9cff-540bc8fbf8a1 | set_id | |
| unii | 4TI98Z838E | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.