escitalopram
- Product NDC
- 67046-1465
- 11-digit product format
- 670461465
- Labeler code
- 67046
- Product ID
- 67046-1465_2d58aaca-22d8-7da2-e063-6394a90af047
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA078777
- Marketing category
- ANDA
- Marketing start
- 2025-02-04
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- escitalopram
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESCITALOPRAM OXALATE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5U85DBW7LO |
| Rxcui | 351250 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-1465-3 | escitalopram | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-1465 | ESCITALOPRAM TABLET, FILM COATED [COUPLER LLC] | 1 | Current NDC, 1 package rows | 20250206_2d58c448-4a6c-1b7d-e063-6294a90a7d03.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 67046-1465-3 | 67046146503 | 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1465-3) | 2025-02-04 | No | No | Historical |