Escitalopram
- Product NDC
- 67296-1528
- 11-digit product format
- 672961528
- Labeler code
- 67296
- Product ID
- 67296-1528_9c9fa3e2-216c-7794-e053-2a95a90a4727
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- 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
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 67296-1528-3 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1528 | ESCITALOPRAM TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20200121_56cf0d87-f81a-309e-e054-00144ff8d46c.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 |
|---|
| 67296-1528-3 | 67296152803 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-1528-3) | 2012-03-14 | 0000-00-00 | No | No | Current |