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Escitalopram Oxalate - 0378-3857-10 - (escitalopram)

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Drug Information of Escitalopram Oxalate

Product NDC: 0378-3857
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: 0378-3857
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021323
Marketing Category: NDA
Start Marketing Date: 20020814

Package Information of Escitalopram Oxalate

Package NDC: 0378-3857-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3857-10)

NDC Information of Escitalopram Oxalate

NDC Code 0378-3857-10
Proprietary Name Escitalopram Oxalate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3857-10)
Product NDC 0378-3857
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 Mylan 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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