Lexapro is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Unit Dose Services. The primary component is Escitalopram Oxalate.
| Product ID | 50436-9803_9270b2e7-ac73-4680-aa5a-00c19c345bca |
| NDC | 50436-9803 |
| 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 | Unit Dose Services |
| Substance Name | ESCITALOPRAM OXALATE |
| Active Ingredient Strength | 10 mg/1 |
| Pharm Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2002-08-14 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021323 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-08-14 |
| Marketing End Date | 2017-12-31 |
| Ingredient | Strength |
|---|---|
| ESCITALOPRAM OXALATE | 10 mg/1 |
| SPL SET ID: | c0813af3-3058-4eb8-8f30-5586d7140864 |
| 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 |