Home > National Drug Code (NDC) > Escitalopram

Escitalopram - 16729-168-10 - (Escitalopram)

Alphabetical Index


Drug Information of Escitalopram

Product NDC: 16729-168
Proprietary Name: Escitalopram
Non Proprietary Name: Escitalopram
Active Ingredient(s): 5    mg/1 & nbsp;   Escitalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Escitalopram

Product NDC: 16729-168
Labeler Name: Accord Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202389
Marketing Category: ANDA
Start Marketing Date: 20130115

Package Information of Escitalopram

Package NDC: 16729-168-10
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16729-168-10)

NDC Information of Escitalopram

NDC Code 16729-168-10
Proprietary Name Escitalopram
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16729-168-10)
Product NDC 16729-168
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130115
Marketing Category Name ANDA
Labeler Name Accord Healthcare Inc.
Substance Name ESCITALOPRAM OXALATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram


General Information