Escitalopram
- Product NDC
- 68788-7510
- 11-digit product format
- 687887510
- Labeler code
- 68788
- Product ID
- 68788-7510_7b1eb291-4462-448b-8c8f-673ae73bb696
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078032
- Marketing category
- ANDA
- Marketing start
- 2012-03-15
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- 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 |
|---|
| 68788-7510 | ESCITALOPRAM TABLET, FILM COATED [PREFERRED PHARMACEUTICALS, INC.] | 7 | Legacy NDC | 20250410_9889f7c0-fe0f-4267-a254-caee9f2b5eb0.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7510-1 | 68788751001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7510-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7510-3 | 68788751003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7510-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7510-6 | 68788751006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7510-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7510-8 | 68788751008 | 28 TABLET, FILM COATED in 1 BOTTLE (68788-7510-8) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7510-9 | 68788751009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7510-9) | 2019-12-27 | 0000-00-00 | No | No | Current |