Escitalopram
- Product NDC
- 70518-2521
- 11-digit product format
- 705182521
- Labeler code
- 70518
- Product ID
- 70518-2521_9b7116be-81f8-31cb-e053-2995a90aaf10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitslopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078169
- Marketing category
- ANDA
- Marketing start
- 2020-01-03
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record