Estradiol
- Product NDC
- 72189-502
- 11-digit product format
- 721890502
- Labeler code
- 72189
- Product ID
- 72189-502_2c4e4735-85f4-83d7-e063-6394a90adcc0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2023-07-27
- 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 |
|---|
| 72189-502-60 | 72189050260 | 60 TABLET in 1 BOTTLE (72189-502-60) | 60 tablet | 2023-07-27 | No | No | Historical |
| 72189-502-90 | 72189050290 | 90 TABLET in 1 BOTTLE (72189-502-90) | 90 tablet | 2023-07-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Estradiol | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL | 3 |