Escitalopram
- Product NDC
- 55154-6649
- 11-digit product format
- 551546649
- Labeler code
- 55154
- Product ID
- 55154-6649_abf6a930-84cd-4055-94dd-8bb019a33676
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA090432
- Marketing category
- ANDA
- Marketing start
- 2013-07-01
- Marketing end
- 2021-03-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-6649-0 | 55154664900 | 10 BLISTER PACK in 1 BAG (55154-6649-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2013-07-01 | 2021-03-31 | No | No | Current |