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Escitalopram Oxalate - 55154-5379-0 - (escitalopram)

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Drug Information of Escitalopram Oxalate

Product NDC: 55154-5379
Proprietary Name: Escitalopram Oxalate
Non Proprietary Name: escitalopram
Active Ingredient(s): 10    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: 55154-5379
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021323
Marketing Category: NDA
Start Marketing Date: 20020814

Package Information of Escitalopram Oxalate

Package NDC: 55154-5379-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5379-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Escitalopram Oxalate

NDC Code 55154-5379-0
Proprietary Name Escitalopram Oxalate
Package Description 10 BLISTER PACK in 1 BAG (55154-5379-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5379
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020814
Marketing Category Name NDA
Labeler Name Cardinal Health
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 Oxalate


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