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NDC 50090-4363-00 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 A-S Medication Solutions. 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: 50090-4363-00
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Escitalopram

Product Information

NDC	50090-4363
Product ID	50090-4363_5a91b076-cfd6-49b3-9beb-808c2f109b26
Associated GPIs	58160034100310
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	A-S Medication Solutions
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 50090-4363-00 (50090436300)

Pricing Information	N/A
NDC Package Code	50090-4363-0
Billing NDC	50090436300
Package	90 TABLET, FILM COATED in 1 BOTTLE (50090-4363-0)
Marketing Start Date	2019-06-17
NDC Exclude Flag	N