Estradiol
- Product NDC
- 50090-7481
- 11-digit product format
- 500907481
- Labeler code
- 50090
- Product ID
- 50090-7481_871f6535-355f-4d32-8dd8-f25c5714ca71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA217334
- Marketing category
- ANDA
- Marketing start
- 2024-07-10
- Substance
- ESTRADIOL
- Active strength
- 1 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 |
|---|
| 50090-7481-0 | 50090748100 | 90 TABLET in 1 BOTTLE (50090-7481-0) | 90 tablet | 2024-12-20 | No | No | Historical |