Escitalopram
- Product NDC
- 68788-9714
- 11-digit product format
- 687889714
- Labeler code
- 68788
- Product ID
- 68788-9714_c807ed8c-073b-4f26-8a57-60a3d0a32838
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA090432
- Marketing category
- ANDA
- Marketing start
- 2013-01-18
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record