Escitalopram Oxalate
- Product NDC
- 55154-5379
- 11-digit product format
- 551545379
- Labeler code
- 55154
- Product ID
- 55154-5379_deda9dc7-a55d-4cd3-a2dd-e6b9bf77bf48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA021323
- Marketing category
- NDA
- Marketing start
- 2002-08-14
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record