Estradiol
- Product NDC
- 50090-2624
- 11-digit product format
- 500902624
- Labeler code
- 50090
- Product ID
- 50090-2624_d9c16a98-0254-4927-b9d7-74b480bf6785
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040326
- Marketing category
- ANDA
- Marketing start
- 1999-06-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2624-0 | 50090262400 | 30 TABLET in 1 BOTTLE (50090-2624-0) | 30 tablet | 2016-11-16 | 0000-00-00 | No | No | Current |