Escitalopram
- Product NDC
- 68001-454
- 11-digit product format
- 680010454
- Labeler code
- 68001
- Product ID
- 68001-454_d619bedd-4bce-5658-e053-2995a90a1f72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2020-10-01
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-454 | ESCITALOPRAM TABLET, FILM COATED [BLUEPOINT LABORATORIES] | 5 | Legacy NDC | 20240207_f95f6759-79f6-4757-9ee0-ff3e233a3721.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-454-00 | 68001045400 | 100 TABLET, FILM COATED in 1 BOTTLE (68001-454-00) | 2020-10-01 | 0000-00-00 | No | No | Current |
| 68001-454-08 | 68001045408 | 1000 TABLET, FILM COATED in 1 BOTTLE (68001-454-08) | 2020-10-01 | 0000-00-00 | No | No | Current |