Escitalopram
- Product NDC
- 64725-1700
- 11-digit product format
- 647251700
- Labeler code
- 64725
- Product ID
- 64725-1700_164c974d-9ffb-498f-8eb6-75fa4627105e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-1700-1 | Escitalopram | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-1700 | ESCITALOPRAM TABLET, FILM COATED [TYA PHARMACEUTICALS] | 8 | Legacy NDC, 1 package rows | 20160619_e0eff3a7-475a-471a-b7c5-256992c5ec1e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-1700-1 | 64725170001 | 100 in 1 BOTTLE | Historical |