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Escitalopram Oxalate - 33342-038-12 - (Escitalopram Oxalate)

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Drug Information of Escitalopram Oxalate

Product NDC: 33342-038
Proprietary Name: Escitalopram Oxalate
Non Proprietary Name: Escitalopram Oxalate
Active Ingredient(s): 20    mg/21 & nbsp;   Escitalopram Oxalate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Escitalopram Oxalate

Product NDC: 33342-038
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202210
Marketing Category: ANDA
Start Marketing Date: 20120911

Package Information of Escitalopram Oxalate

Package NDC: 33342-038-12
Package Description: 100 TABLET, FILM COATED in 1 CARTON (33342-038-12)

NDC Information of Escitalopram Oxalate

NDC Code 33342-038-12
Proprietary Name Escitalopram Oxalate
Package Description 100 TABLET, FILM COATED in 1 CARTON (33342-038-12)
Product NDC 33342-038
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram Oxalate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120911
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name ESCITALOPRAM OXALATE
Strength Number 20
Strength Unit mg/21
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram Oxalate


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