Home > National Drug Code (NDC) > Escitalopram Oxalate

Escitalopram Oxalate - 54868-6375-0 - (escitalopram)

Alphabetical Index


Drug Information of Escitalopram Oxalate

Product NDC: 54868-6375
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: 54868-6375
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021323
Marketing Category: NDA
Start Marketing Date: 20121016

Package Information of Escitalopram Oxalate

Package NDC: 54868-6375-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-6375-0)

NDC Information of Escitalopram Oxalate

NDC Code 54868-6375-0
Proprietary Name Escitalopram Oxalate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-6375-0)
Product NDC 54868-6375
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121016
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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


General Information