Escitalopram
- Product NDC
- 51655-149
- 11-digit product format
- 516550149
- Labeler code
- 51655
- Product ID
- 51655-149_48c3f3e4-25a2-6aa7-e063-6394a90a0057
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2021-05-07
- 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
- 2027-12-31
- Current FDA listing
- Yes
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-149-26 | Escitalopram | 90 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 90 | | 4 |
| 51655-149-52 | Escitalopram | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-149 | ESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Current NDC, 2 package rows | 20241225_d9ba6c65-22bd-10c4-e053-2995a90ada2e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-149-26 | 51655014926 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-26) | 2022-02-09 | No | No | Historical |
| 51655-149-52 | 51655014952 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-149-52) | 2021-05-07 | No | No | Historical |