escitalopram oxalate
- Product NDC
- 50090-1279
- 11-digit product format
- 500901279
- Labeler code
- 50090
- Product ID
- 50090-1279_22f30729-a6d4-4632-a6d0-8b18d8cef7fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram oxalate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1279 | ESCITALOPRAM OXALATE TABLET [A-S MEDICATION SOLUTIONS] | 11 | Legacy NDC | 20240103_64399589-23db-4036-9d14-c29ce5808bb1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1279-0 | 50090127900 | 30 TABLET in 1 BOTTLE (50090-1279-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-1279-1 | 50090127901 | 90 TABLET in 1 BOTTLE (50090-1279-1) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |