Escitalopram
- Product NDC
- 45865-787
- 11-digit product format
- 458650787
- Labeler code
- 45865
- Product ID
- 45865-787_7d77134c-20dd-39e8-e053-2991aa0a4a3b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- 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 |
|---|
| 45865-787-30 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-787 | ESCITALOPRAM TABLET, FILM COATED [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20181221_7d77134c-20dc-39e8-e053-2991aa0a4a3b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 45865-787-30 | 45865078730 | 30 in 1 BOTTLE | Historical |