escitalopram
- Product NDC
- 71335-2460
- 11-digit product format
- 713352460
- Labeler code
- 71335
- Product ID
- 71335-2460_8ce8cbca-a1cc-455c-86e1-03a698d5f0d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- escitalopram
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| ESCITALOPRAM OXALATE | 5 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 5U85DBW7LO |
| Rxcui | 351249 |
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 |
|---|
| 71335-2460-1 | 71335246001 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2460-1) | 2024-09-27 | No | No | Current |
| 71335-2460-2 | 71335246002 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2460-2) | 2024-12-12 | No | No | Current |
| 71335-2460-3 | 71335246003 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2460-3) | 2024-07-29 | No | No | Current |
| 71335-2460-4 | 71335246004 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2460-4) | 2024-12-12 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| escitalopram | Bryant Ranch Prepack | 2024-12-12 | HUMAN PRESCRIPTION DRUG LABEL | 2 |