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escitalopram oxalate - 13668-135-05 - (escitalopram oxalate)

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Drug Information of escitalopram oxalate

Product NDC: 13668-135
Proprietary Name: escitalopram oxalate
Non Proprietary Name: escitalopram oxalate
Active Ingredient(s): 5    mg/1 & nbsp;   escitalopram oxalate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of escitalopram oxalate

Product NDC: 13668-135
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090939
Marketing Category: ANDA
Start Marketing Date: 20120911

Package Information of escitalopram oxalate

Package NDC: 13668-135-05
Package Description: 500 TABLET in 1 BOTTLE (13668-135-05)

NDC Information of escitalopram oxalate

NDC Code 13668-135-05
Proprietary Name escitalopram oxalate
Package Description 500 TABLET in 1 BOTTLE (13668-135-05)
Product NDC 13668-135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name escitalopram oxalate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120911
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name ESCITALOPRAM OXALATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of escitalopram oxalate


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