ESTRADIOL
- Product NDC
- 50090-6363
- 11-digit product format
- 500906363
- Labeler code
- 50090
- Product ID
- 50090-6363_ba221d24-d90d-40f3-a19e-2bcc303c70df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESTRADIOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2017-04-10
- Substance
- ESTRADIOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4TI98Z838E | ESTRADIOL | 50-28-2 | ESTRADIOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6363-0 | 50090636300 | 30 TABLET in 1 BOTTLE (50090-6363-0) | 30 tablet | 2023-02-09 | No | No | Historical |
| 50090-6363-2 | 50090636302 | 90 TABLET in 1 BOTTLE (50090-6363-2) | 90 tablet | 2025-02-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Estradiol Tablets, USP | A-S Medication Solutions | 2025-02-18 | HUMAN PRESCRIPTION DRUG LABEL | 3 |