Escitalopram
- Product NDC
- 68788-6403
- 11-digit product format
- 687886403
- Labeler code
- 68788
- Product ID
- 68788-6403_4ba94e2d-30cc-4a0e-8839-185dcfc147e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2016-06-09
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record