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NDC 71205-0325-90 Escitalopram 20 mg/1 Details

Escitalopram 20 mg/1

Escitalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. 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: 71205-0325-90
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Escitalopram

Product Information

NDC	71205-0325
Product ID	71205-325_65ffd6fd-533b-4e39-8fbc-5c65cd88d602
Associated GPIs	58160034100330
GCN Sequence Number	050760
GCN Sequence Number Description	escitalopram oxalate TABLET 20 MG ORAL
HIC3	H2S
HIC3 Description	SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
GCN	17987
HICL Sequence Number	024022
HICL Sequence Number Description	ESCITALOPRAM OXALATE
Brand/Generic	Generic
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	20
Active Ingredient Units	mg/1
Substance Name	ESCITALOPRAM OXALATE
Labeler Name	Proficient Rx LP
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 71205-0325-90 (71205032590)

Pricing Information	N/A
NDC Package Code	71205-325-90
Billing NDC	71205032590
Package	90 TABLET, FILM COATED in 1 BOTTLE (71205-325-90)
Marketing Start Date	2019-09-01
NDC Exclude Flag	N