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Escitalopram oxalate - 76282-251-30 - (escitalopram)

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Drug Information of Escitalopram oxalate

Product NDC: 76282-251
Proprietary Name: Escitalopram oxalate
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 oxalate

Product NDC: 76282-251
Labeler Name: Exelan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078604
Marketing Category: ANDA
Start Marketing Date: 20121001

Package Information of Escitalopram oxalate

Package NDC: 76282-251-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (76282-251-30)

NDC Information of Escitalopram oxalate

NDC Code 76282-251-30
Proprietary Name Escitalopram oxalate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (76282-251-30)
Product NDC 76282-251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121001
Marketing Category Name ANDA
Labeler Name Exelan Pharmaceuticals 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 oxalate


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