Escitalopram
- Product NDC
- 57237-094
- 11-digit product format
- 572370094
- Labeler code
- 57237
- Product ID
- 57237-094_12f6a619-58cb-4428-bfa5-66859253efed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA090432
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record