escitalopram
- Product NDC
- 60760-894
- 11-digit product format
- 607600894
- Labeler code
- 60760
- Product ID
- 60760-894_3623240f-a96f-d97b-e063-6394a90a9ab6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA078777
- Marketing category
- ANDA
- Marketing start
- 2023-06-10
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5U85DBW7LO | ESCITALOPRAM OXALATE | 219861-08-2 | ESCITALOPRAM OXALATE |
| 4O4S742ANY | ESCITALOPRAM | 128196-01-0 | escitalopram |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-894-30 | 60760089430 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-894-30) | 2025-05-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| escitalopram | ST. MARY'S MEDICAL PARK PHARMACY | 2025-05-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |