Lexapro is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Escitalopram Oxalate.
| Product ID | 63629-2981_4a08b6cf-7ba0-54a9-14e0-a6e8d1e4854e | 
| NDC | 63629-2981 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Lexapro | 
| Generic Name | Escitalopram Oxalate | 
| Dosage Form | Tablet, Film Coated | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2002-08-14 | 
| Marketing Category | NDA / NDA | 
| Application Number | NDA021323 | 
| Labeler Name | Bryant Ranch Prepack | 
| Substance Name | ESCITALOPRAM OXALATE | 
| Active Ingredient Strength | 20 mg/1 | 
| Pharm Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2023-12-31 | 
| Marketing Start Date | 2005-10-25 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | NDA | 
| Application Number | NDA021323 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2005-10-25 | 
| Marketing Category | NDA | 
| Application Number | NDA021323 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2005-10-25 | 
| Marketing Category | NDA | 
| Application Number | NDA021323 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2005-10-25 | 
| Ingredient | Strength | 
|---|---|
| ESCITALOPRAM OXALATE | 20 mg/1 | 
| SPL SET ID: | 4a08b6cf-7ba0-54a9-14e0-a6e8d1e4854e | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0456-2005 | Lexapro | ESCITALOPRAM | 
| 0456-2010 | Lexapro | ESCITALOPRAM | 
| 0456-2020 | Lexapro | ESCITALOPRAM | 
| 33261-699 | Lexapro | Lexapro | 
| 33261-686 | Lexapro | Lexapro | 
| 50436-9803 | Lexapro | Lexapro | 
| 55289-768 | Lexapro | Lexapro | 
| 55289-828 | Lexapro | Lexapro | 
| 63629-2981 | Lexapro | Lexapro | 
| 0121-0852 | Escitalopram Oxalate | Escitalopram Oxalate | 
| 0904-6426 | escitalopram oxalate | escitalopram oxalate | 
| 0904-6427 | escitalopram oxalate | escitalopram oxalate | 
| 10544-224 | escitalopram oxalate | escitalopram oxalate | 
| 10544-225 | escitalopram oxalate | escitalopram oxalate | 
| 10544-230 | escitalopram oxalate | escitalopram oxalate | 
| 13668-135 | escitalopram oxalate | escitalopram oxalate | 
| 13668-136 | escitalopram oxalate | escitalopram oxalate | 
| 13668-137 | escitalopram oxalate | escitalopram oxalate | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  LEXAPRO  79388487  not registered Live/Pending | H. Lundbeck A/S 2023-11-23 | 
|  LEXAPRO  76184942  2684432 Live/Registered | H. Lundbeck A/S 2000-12-22 |