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Escitalopram - 49349-950-24 - (Escitalopram)

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Drug Information of Escitalopram

Product NDC: 49349-950
Proprietary Name: Escitalopram
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

Product NDC: 49349-950
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076765
Marketing Category: ANDA
Start Marketing Date: 20130218

Package Information of Escitalopram

Package NDC: 49349-950-24
Package Description: 200 TABLET, FILM COATED in 1 CANISTER (49349-950-24)

NDC Information of Escitalopram

NDC Code 49349-950-24
Proprietary Name Escitalopram
Package Description 200 TABLET, FILM COATED in 1 CANISTER (49349-950-24)
Product NDC 49349-950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130218
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


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