Escitalopram
- Product NDC
- 0615-8476
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA090432
- Marketing category
- ANDA
- Substance
- ESCITALOPRAM OXALATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0615-8476-05 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-05) | 2023-05-10 | | No | Historical |
| 0615-8476-28 | 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28) | 2025-01-15 | | No | Historical |
| 0615-8476-39 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-39) | 2023-05-10 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Escitalopram | NCS HealthCare of KY, LLC dba Vangard Labs | 2025-01-24 | HUMAN PRESCRIPTION DRUG LABEL | 4 |