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Escitalopram - 60505-2781-0 - (Escitalopram Oxalate)

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Drug Information of Escitalopram

Product NDC: 60505-2781
Proprietary Name: Escitalopram
Non Proprietary Name: Escitalopram Oxalate
Active Ingredient(s): 10    mg/1 & nbsp;   Escitalopram Oxalate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Escitalopram

Product NDC: 60505-2781
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078777
Marketing Category: ANDA
Start Marketing Date: 20120911

Package Information of Escitalopram

Package NDC: 60505-2781-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2781-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Escitalopram

NDC Code 60505-2781-0
Proprietary Name Escitalopram
Package Description 10 BLISTER PACK in 1 CARTON (60505-2781-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-2781
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram Oxalate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120911
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name ESCITALOPRAM OXALATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram


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