Escitalopram
- Product NDC
- 50090-3331
- 11-digit product format
- 500903331
- Labeler code
- 50090
- Product ID
- 50090-3331_b314da5b-2cc7-4161-b60d-9db5d97ad2b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-3331-0 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 6 |
| 50090-3331-1 | Escitalopram | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3331 | ESCITALOPRAM TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 2 package rows | 20210303_88d77d84-7349-4af4-81ca-d5fd5099b7c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3331-0 | 50090333100 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3331-0) | 2018-01-15 | 0000-00-00 | No | No | Current |
| 50090-3331-1 | 50090333101 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3331-1) | 2018-02-16 | 0000-00-00 | No | No | Current |