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NDC 51655-0766-52 Escitalopram 5 mg/1 Details

Escitalopram 5 mg/1

Escitalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. 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: 51655-0766-52
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Escitalopram

Product Information

NDC	51655-0766
Product ID	51655-766_da7feb56-5f59-7487-e053-2995a90a119e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Escitalopram
Proprietary Name Suffix	n/a
Non-Proprietary Name	Escitalopram
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	ESCITALOPRAM OXALATE
Labeler Name	Northwind Pharmaceuticals
Pharmaceutical Class	Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202389
Listing Certified Through	2024-12-31

Package

NDC 51655-0766-52 (51655076652)

Pricing Information	N/A
NDC Package Code	51655-766-52
Billing NDC	51655076652
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-766-52)
Marketing Start Date	2021-07-27
NDC Exclude Flag	N