Escitalopram Oxalate
- Product NDC
- 50090-7201
- 11-digit product format
- 500907201
- Labeler code
- 50090
- Product ID
- 50090-7201_53eb97bf-6b7e-4879-90cc-98fd0c327a40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202210
- Marketing category
- ANDA
- Marketing start
- 2024-01-08
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 mg/21
- 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 |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7201-0 | 50090720100 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7201-0) | 2024-07-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Escitalopram Oxalate | A-S Medication Solutions | 2024-07-31 | Human Prescription Drug Label | 1 |