Escitalopram
- Product NDC
- 50090-5703
- 11-digit product format
- 500905703
- Labeler code
- 50090
- Product ID
- 50090-5703_8e5317fe-0f0e-46f6-80e9-a61c8dde737e
- 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
- 10 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5703-0 | 50090570300 | 30 TABLET in 1 BOTTLE (50090-5703-0) | 30 tablet | 2021-09-23 | 0000-00-00 | No | No | Current |
| 50090-5703-1 | 50090570301 | 90 TABLET in 1 BOTTLE (50090-5703-1) | 90 tablet | 2021-09-23 | 0000-00-00 | No | No | Current |