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NDC 65162-0021-50 Escitalopram Oxalate 20 mg/1 Details

Escitalopram Oxalate 20 mg/1

Escitalopram Oxalate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals 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. 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: 65162-0021-50
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Escitalopram

Product Information

NDC	65162-0021
Product ID	65162-021_c88e0081-6db8-468c-90cb-205a3c2e7eea
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 Oxalate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Escitalopram Oxalate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	ESCITALOPRAM OXALATE
Labeler Name	Amneal Pharmaceuticals LLC
Pharmaceutical Class	Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA205619
Listing Certified Through	2024-12-31

Package

NDC 65162-0021-50 (65162002150)

Pricing Information	N/A
NDC Package Code	65162-021-50
Billing NDC	65162002150
Package	500 TABLET, FILM COATED in 1 BOTTLE (65162-021-50)
Marketing Start Date	2017-05-17
NDC Exclude Flag	N