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NDC 68788-7461-09 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 Preferred Pharmaceuticals, Inc.. 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: 68788-7461-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Escitalopram

Product Information

NDC	68788-7461
Product ID	68788-7461_340198fd-4d37-4b67-bf4e-038a0e77d2c1
Associated GPIs	58160034100330
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	20
Active Ingredient Units	mg/1
Substance Name	ESCITALOPRAM OXALATE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078032
Listing Certified Through	2024-12-31

Package

NDC 68788-7461-09 (68788746109)

Pricing Information	N/A
NDC Package Code	68788-7461-9
Billing NDC	68788746109
Package	90 TABLET, FILM COATED in 1 BOTTLE (68788-7461-9)
Marketing Start Date	2019-12-27
NDC Exclude Flag	N