Escitalopram
- Product NDC
- 68788-7559
- 11-digit product format
- 687887559
- Labeler code
- 68788
- Product ID
- 68788-7559_ddce18c6-ab27-4f2e-a5e3-65b213b9bb95
- 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
- 5 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7559-1 | 68788755901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7559-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7559-3 | 68788755903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7559-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7559-6 | 68788755906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7559-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7559-8 | 68788755908 | 28 TABLET, FILM COATED in 1 BOTTLE (68788-7559-8) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7559-9 | 68788755909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7559-9) | 2019-12-27 | 0000-00-00 | No | No | Current |