ESTRADIOL
- Product NDC
- 70934-798
- 11-digit product format
- 709340798
- Labeler code
- 70934
- Product ID
- 70934-798_b2ac23b3-bf48-3847-e053-2995a90afdd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESTRADIOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2020-10-19
- Marketing end
- 0000-00-00
- Substance
- ESTRADIOL
- Active strength
- 1 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-798-30 | 70934079830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-798-30) | 30 tablet | 2020-10-19 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Estradiol Tablets, USP | Denton Pharma, Inc. dba Northwind Pharmaceuticals | 2020-10-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |