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NDC 62135-0729-37 Escitalopram Oral Solution 5 mg/5mL Details
Escitalopram Oral Solution 5 mg/5mL
Escitalopram Oral Solution is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is ESCITALOPRAM OXALATE.
MedlinePlus Drug Summary
Escitalopram is used to treat depression in adults and children and teenagers 12 years of ago or older. Escitalopram is also used to treat generalized anxiety disorder (GAD; excessive worry and tension that disrupts daily life and lasts for 6 months or longer) in adults, teenagers, and children 7 years of age and older. Escitalopram is in a class of antidepressants called selective serotonin reuptake inhibitors (SSRIs). It works by increasing the amount of serotonin, a natural substance in the brain that helps maintain mental balance.
Related Packages: 62135-0729-37Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Escitalopram
Product Information
| NDC | 62135-0729 |
|---|---|
| Product ID | 62135-729_0451d0ef-4b6f-a01b-e063-6294a90a9323 |
| Associated GPIs | |
| GCN Sequence Number | 051698 |
| GCN Sequence Number Description | escitalopram oxalate SOLUTION 5 MG/5 ML ORAL |
| HIC3 | H2S |
| HIC3 Description | SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS) |
| GCN | 19035 |
| HICL Sequence Number | 024022 |
| HICL Sequence Number Description | ESCITALOPRAM OXALATE |
| Brand/Generic | Generic |
| Proprietary Name | Escitalopram Oral Solution |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Escitalopram Oral |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/5mL |
| Substance Name | ESCITALOPRAM OXALATE |
| Labeler Name | Chartwell RX, LLC |
| Pharmaceutical Class | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA090477 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 62135-0729-37 (62135072937)
| NDC Package Code | 62135-729-37 |
|---|---|
| Billing NDC | 62135072937 |
| Package | 240 mL in 1 BOTTLE (62135-729-37) |
| Marketing Start Date | 2023-08-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |