escitalopram oxalate
- Product NDC
- 68071-4210
- 11-digit product format
- 680714210
- Labeler code
- 68071
- Product ID
- 68071-4210_61f93369-375d-276e-e053-2991aa0ad11d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram oxalate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record