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Escitalopram - 0093-5851-93 - (Escitalopram)

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Drug Information of Escitalopram

Product NDC: 0093-5851
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: 0093-5851
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076765
Marketing Category: ANDA
Start Marketing Date: 20120314

Package Information of Escitalopram

Package NDC: 0093-5851-93
Package Description: 100 BLISTER PACK in 1 BOX (0093-5851-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-5851-19)

NDC Information of Escitalopram

NDC Code 0093-5851-93
Proprietary Name Escitalopram
Package Description 100 BLISTER PACK in 1 BOX (0093-5851-93) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-5851-19)
Product NDC 0093-5851
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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