Estradiol
- Product NDC
- 55289-761
- 11-digit product format
- 552890761
- Labeler code
- 55289
- Product ID
- 55289-761_a82360f3-f6d7-0c0b-e053-2995a90abe7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040326
- Marketing category
- ANDA
- Marketing start
- 1999-06-17
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55289-761-01 | 55289076101 | 100 TABLET in 1 BOTTLE, PLASTIC (55289-761-01) | 100 tablet | 2009-12-21 | 0000-00-00 | No | No | Current |
| 55289-761-30 | 55289076130 | 30 TABLET in 1 BOTTLE, PLASTIC (55289-761-30) | 30 tablet | 2009-12-21 | 0000-00-00 | No | No | Current |
| 55289-761-90 | 55289076190 | 90 TABLET in 1 BOTTLE, PLASTIC (55289-761-90) | 90 tablet | 2009-12-21 | 0000-00-00 | No | No | Current |