Escitalopram
- Product NDC
- 42708-023
- 11-digit product format
- 427080023
- Labeler code
- 42708
- Product ID
- 42708-023_bd5ac5c0-0708-47f0-e053-2995a90a2d65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42708-023-30 | 42708002330 | 30 TABLET, FILM COATED in 1 BOTTLE (42708-023-30) | 2018-03-14 | 0000-00-00 | Yes | No | Current |