Escitalopram
- Product NDC
- 50090-1930
- 11-digit product format
- 500901930
- Labeler code
- 50090
- Product ID
- 50090-1930_b6364140-e77a-47a5-9b0e-05a6c1e21dd9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-21
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1930 | ESCITALOPRAM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 21 | Legacy NDC | 20240425_b2e9d35e-0157-47f1-a31a-6a1f431b5fde.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1930-0 | 50090193000 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1930-0) | 2015-07-16 | 0000-00-00 | No | No | Current |
| 50090-1930-1 | 50090193001 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-1930-1) | 2015-07-16 | 0000-00-00 | No | No | Current |