ESTRADIOL
- Product NDC
- 68788-7567
- 11-digit product format
- 687887567
- Labeler code
- 68788
- Product ID
- 68788-7567_e53d66bc-c827-4b8b-8f9f-b7236597cddc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESTRADIOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2017-04-10
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7567-1 | 68788756701 | 100 TABLET in 1 BOTTLE (68788-7567-1) | 100 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7567-3 | 68788756703 | 30 TABLET in 1 BOTTLE (68788-7567-3) | 30 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7567-6 | 68788756706 | 60 TABLET in 1 BOTTLE (68788-7567-6) | 60 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7567-9 | 68788756709 | 90 TABLET in 1 BOTTLE (68788-7567-9) | 90 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |