Escitalopram
- Product NDC
- 63629-6351
- 11-digit product format
- 636296351
- Labeler code
- 63629
- Product ID
- 63629-6351_831ceda7-0529-43a8-8768-21eb18b2fe42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- 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
- 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 |
|---|
| 63629-6351-1 | 63629635101 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6351-1) | 2015-09-04 | 0000-00-00 | No | No | Current |
| 63629-6351-2 | 63629635102 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-6351-2) | 2015-09-04 | 0000-00-00 | No | No | Current |