Escitalopram
- Product NDC
- 70518-2504
- 11-digit product format
- 705182504
- Labeler code
- 70518
- Product ID
- 70518-2504_9a6a2c6b-7c12-48b1-e053-2a95a90a6910
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202280
- Marketing category
- ANDA
- Marketing start
- 2019-12-23
- 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