Escitalopram
- Product NDC
- 50090-5831
- 11-digit product format
- 500905831
- Labeler code
- 50090
- Product ID
- 50090-5831_53f2ff49-34a2-4c23-ac26-05594ac2e8ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitslopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078169
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 mg/1
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5831-0 | 50090583100 | 32 BLISTER PACK in 1 CARTON (50090-5831-0) > 1 TABLET in 1 BLISTER PACK | 32 blister pack | 2021-10-26 | 0000-00-00 | No | No | Current |