ESTRADIOL
- Product NDC
- 68788-7332
- 11-digit product format
- 687887332
- Labeler code
- 68788
- Product ID
- 68788-7332_0d739b45-79ff-4c24-b526-3777f3903005
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESTRADIOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040275
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7332 | ESTRADIOL TABLET [PREFERRED PHARMACEUTICALS INC.] | 7 | Legacy NDC | 20250502_ac3e9642-2c77-4f2a-ba0f-5276d1055c76.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7332-1 | 68788733201 | 100 TABLET in 1 BOTTLE (68788-7332-1) | 100 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7332-3 | 68788733203 | 30 TABLET in 1 BOTTLE (68788-7332-3) | 30 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7332-6 | 68788733206 | 60 TABLET in 1 BOTTLE (68788-7332-6) | 60 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7332-9 | 68788733209 | 90 TABLET in 1 BOTTLE (68788-7332-9) | 90 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |