ESCITALOPRAM OXALATE
- Product NDC
- 61919-028
- 11-digit product format
- 619190028
- Labeler code
- 61919
- Product ID
- 61919-028_75d1dc2e-d527-4889-8eee-2be9443b644b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ESCITALOPRAM OXALATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 61919-028-30 | ESCITALOPRAM OXALATE | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-028 | ESCITALOPRAM OXALATE TABLET [DIRECT RX] | 6 | Legacy NDC, 1 package rows | 20150811_dfe724f8-c6f3-4f0f-8466-4abce161f15a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-028-30 | 61919002830 | 30 in 1 BOTTLE | Historical |