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Escitalopram - 31722-250-01 - (Escitalopram)

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Drug Information of Escitalopram

Product NDC: 31722-250
Proprietary Name: Escitalopram
Non Proprietary Name: Escitalopram
Active Ingredient(s): 10    mg/1 & nbsp;   Escitalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Escitalopram

Product NDC: 31722-250
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078604
Marketing Category: ANDA
Start Marketing Date: 20120911

Package Information of Escitalopram

Package NDC: 31722-250-01
Package Description: 100 TABLET in 1 BOTTLE (31722-250-01)

NDC Information of Escitalopram

NDC Code 31722-250-01
Proprietary Name Escitalopram
Package Description 100 TABLET in 1 BOTTLE (31722-250-01)
Product NDC 31722-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120911
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
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


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