Lexapro
- Product NDC
- 63629-2981
- 11-digit product format
- 636292981
- Labeler code
- 63629
- Product ID
- 63629-2981_4a08b6cf-7ba0-54a9-14e0-a6e8d1e4854e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESCITALOPRAM OXALATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021323
- Marketing category
- NDA
- Marketing start
- 2002-08-14
- 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
- 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 |
|---|
| 63629-2981-1 | 63629298101 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-2981-1) | 2005-10-25 | 0000-00-00 | No | No | Current |
| 63629-2981-2 | 63629298102 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-2981-2) | 2010-03-24 | 0000-00-00 | No | No | Current |
| 63629-2981-3 | 63629298103 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-2981-3) | 2011-12-13 | 0000-00-00 | No | No | Current |