Estradiol Benzoate
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2025-07-15
- Label type
- BULK INGREDIENT - ANIMAL DRUG
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:51:53
Label at a glance#
ProductEstradiol Benzoate
Active ingredientESTRADIOL BENZOATE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73377-147-01 | Estradiol Benzoate | 50 g in 1 JAR | POWDER | 50 | 2 | |
| 73377-147-02 | Estradiol Benzoate | 100 g in 1 PACKAGE | POWDER | 100 | 2 |
Products#
Every source-derived product name is available through these pages.
- Estradiol Benzoate
- ESTRADIOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73377-147 | 73377-147-01, 73377-147-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ESTRADIOL BENZOATE | 1S4CJB5ZGN | ACTIB |
Source Document#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

