Escitalopram Oxalate
- Product NDC
- 17856-0551
- 11-digit product format
- 178560551
- Labeler code
- 17856
- Product ID
- 17856-0551_7ca31e74-88a6-4a71-914c-839e2b16868f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP
- Application
- ANDA090477
- Marketing category
- ANDA
- Marketing start
- 2013-05-30
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0551-1 | 17856055101 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0551-1) > 5 mL in 1 CUP, UNIT-DOSE | 2021-01-22 | 0000-00-00 | No | No | Current |