Escitalopram
- Product NDC
- 0143-9809
- 11-digit product format
- 001439809
- Labeler code
- 0143
- Product ID
- 0143-9809_322655e3-fff3-4292-abf5-fb9634227072
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- West-Ward Pharmaceuticals Corp
- Application
- ANDA078766
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record