Escitalopram
- Product NDC
- 50436-0170
- 11-digit product format
- 504360170
- Labeler code
- 50436
- Product ID
- 50436-0170_f39b56f8-ce93-48cf-9ee0-264bf89a83df
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Unit Dose Services
- 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
- 2020-12-31
- 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 |
|---|
| 50436-0170-1 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0170 | ESCITALOPRAM TABLET, FILM COATED [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20190106_fc0104ef-13b9-4414-8c26-2e989d37ab0b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0170-1 | 50436017001 | 30 in 1 BOTTLE | Historical |