escitalopram
- Product NDC
- 71335-2903
- 11-digit product format
- 713352903
- Labeler code
- 71335
- Product ID
- 71335-2903_72212dba-b9a9-4385-972c-9f6300227a1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- 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
- 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 |
|---|
| 71335-2903-1 | 71335290301 | 1000 TABLET, FILM COATED in 1 BOTTLE (71335-2903-1) | 2025-10-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| escitalopram | Bryant Ranch Prepack | 2025-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 100 |