Escitalopram
- Product NDC
- 50090-4363
- 11-digit product format
- 500904363
- Labeler code
- 50090
- Product ID
- 50090-4363_3c6fe745-5c82-4336-8aa6-a16ef1d7a461
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-05
- 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
- 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 |
|---|
| 50090-4363-0 | 50090436300 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4363-0) | 2019-06-17 | 0000-00-00 | No | No | Current |