Escitalopram Oxalate
- Product NDC
- 0121-0852
- 11-digit product format
- 001210852
- Labeler code
- 0121
- Product ID
- 0121-0852_ed852c05-8604-dbed-e053-2995a90a5de0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA090477
- Marketing category
- ANDA
- Marketing start
- 2013-05-30
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 10 mg/10mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0852-40 | 00121085240 | 4 TRAY in 1 CASE (0121-0852-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (0121-0852-10) | 4 tray | 2018-06-04 | 0000-00-00 | No | No | Current |