Escitalopram Oxalate
- Product NDC
- 68645-520
- 11-digit product format
- 686450520
- Labeler code
- 68645
- Product ID
- 68645-520_4cc2fbda-eb50-c09c-e063-6394a90a9315
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA078604
- Marketing category
- ANDA
- Marketing start
- 2016-06-16
- Marketing end
- 2027-08-31
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Escitalopram Oxalate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESCITALOPRAM OXALATE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5U85DBW7LO |
| Rxcui | 349332, 351250 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68645-520-54 | Escitalopram Oxalate | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-520 | ESCITALOPRAM OXALATE (ESCITALOPRAM) TABLET, FILM COATED [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250125_9c68f89b-1d34-4735-9631-817f012935d7.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 |
|---|
| 68645-520-54 | 68645052054 | 30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54) | 2016-06-16 | 2027-08-31 | No | No | Current |