Estradiol
- Product NDC
- 68071-2487
- 11-digit product format
- 680712487
- Labeler code
- 68071
- Product ID
- 68071-2487_3f679615-ebb4-453e-e063-6294a90a0dd8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040197
- Marketing category
- ANDA
- Marketing start
- 1997-10-28
- 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 |
|---|
| 68071-2487-3 | 68071248703 | 30 TABLET in 1 BOTTLE (68071-2487-3) | 30 tablet | 2021-08-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Estradiol Tablets USP | NuCare Pharmaceuticals,Inc. | 2025-09-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |