Escitalopram
- Product NDC
- 50090-5131
- 11-digit product format
- 500905131
- Labeler code
- 50090
- Product ID
- 50090-5131_15393573-e952-4352-964a-34f87333ab1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090432
- 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
- 2021-12-31
- 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 |
|---|
| 50090-5131-0 | Escitalopram | 33 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 33 | | 1 |
| 50090-5131-0 | Escitalopram | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5131 | ESCITALOPRAM (ESCITALOPRAM OXALATE) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20200822_07c7a6b2-44cb-4808-9892-496e80f1d9c2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5131-0 | 50090513100 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-5131-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 33 blister pack | 2020-08-14 | 0000-00-00 | No | No | Current |