Estradiol
- Product NDC
- 43063-706
- 11-digit product format
- 430630706
- Labeler code
- 43063
- Product ID
- 43063-706_dc7a1972-ab0f-d2fe-e053-2a95a90a0544
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040197
- Marketing category
- ANDA
- Marketing start
- 2016-08-03
- Marketing end
- 0000-00-00
- Substance
- ESTRADIOL
- Active strength
- 1 mg/1
- Pharmacologic classes
- Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 43063-706-30 | 43063070630 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-706-30) | 30 tablet | 2016-10-06 | 0000-00-00 | No | No | Current |
| 43063-706-90 | 43063070690 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-706-90) | 90 tablet | 2016-09-20 | 0000-00-00 | No | No | Current |