Escitalopram
- Product NDC
- 67296-1200
- 11-digit product format
- 672961200
- Labeler code
- 67296
- Product ID
- 67296-1200_d610062d-3995-dec3-e053-2995a90a9ca1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-19
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1200-3 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
| 67296-1200-9 | Escitalopram | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1200 | ESCITALOPRAM TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 2 package rows | 20220121_4ecd48c4-482a-5681-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 |
|---|
| 67296-1200-3 | 67296120003 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-1200-3) | 2013-03-19 | 0000-00-00 | No | No | Current |
| 67296-1200-9 | 67296120009 | 90 TABLET, FILM COATED in 1 BOTTLE (67296-1200-9) | 2013-03-19 | 0000-00-00 | No | No | Current |