ESTRADIOL
- Product NDC
- 51655-860
- 11-digit product format
- 516550860
- Labeler code
- 51655
- Product ID
- 51655-860_4bbc8ae6-5a91-a88b-e063-6294a90a809f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESTRADIOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2023-02-09
- Substance
- ESTRADIOL
- Active strength
- .5 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 51655-860-26 | 51655086026 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-860-26) | 90 tablet | 2023-05-04 | No | No | Historical |
| 51655-860-52 | 51655086052 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-860-52) | 30 tablet | 2023-02-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Estradiol Tablets, USP | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 5 |