Escitalopram
- Product NDC
- 71335-2058
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202389
- Marketing category
- ANDA
- Substance
- ESCITALOPRAM OXALATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-2058-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2058-1) | 20220630 | | No | Historical |
| 71335-2058-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2058-2) | 20250131 | | No | Historical |
| 71335-2058-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2058-3) | 20220304 | | No | Historical |
| 71335-2058-4 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2058-4) | 20250131 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 43eb9e4f-1a46-46f7-9e9d-43e866963b37 | These highlights do not include all the information needed to use ESCITALOPRAM TABLETS safely and effectively. See full prescribing information for ESCITALOPRAM TABLETS. ESCITALOPRAM tablets, for oral use Initial U.S. Approval: 2002 | Bryant Ranch Prepack | 2025-01-31 | HUMAN PRESCRIPTION DRUG LABEL | 103 |