Estradiol
- Product NDC
- 51862-334
- 11-digit product format
- 518620334
- Labeler code
- 51862
- Product ID
- 51862-334_82bf095a-96f7-49e1-9946-53eb3cad9989
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA040197
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- Marketing end
- 0000-00-00
- Substance
- ESTRADIOL
- Active strength
- 2 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51862-334-01 | 51862033401 | 100 TABLET in 1 BOTTLE (51862-334-01) | 100 tablet | 2016-08-03 | 0000-00-00 | No | No | Current |
| 51862-334-05 | 51862033405 | 500 TABLET in 1 BOTTLE (51862-334-05) | 500 tablet | 2016-08-03 | 0000-00-00 | No | No | Current |