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Escitalopram - 16729-170-17 - (Escitalopram)

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Drug Information of Escitalopram

Product NDC: 16729-170
Proprietary Name: Escitalopram
Non Proprietary Name: Escitalopram
Active Ingredient(s): 20    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: 16729-170
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: 16729-170-17
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)

NDC Information of Escitalopram

NDC Code 16729-170-17
Proprietary Name Escitalopram
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (16729-170-17)
Product NDC 16729-170
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 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram


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