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Escitalopram - 0143-9807-05 - (Escitalopram)

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Drug Information of Escitalopram

Product NDC: 0143-9807
Proprietary Name: Escitalopram
Non Proprietary Name: Escitalopram
Active Ingredient(s): 20    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: 0143-9807
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078766
Marketing Category: ANDA
Start Marketing Date: 20120911

Package Information of Escitalopram

Package NDC: 0143-9807-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9807-05)

NDC Information of Escitalopram

NDC Code 0143-9807-05
Proprietary Name Escitalopram
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9807-05)
Product NDC 0143-9807
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Escitalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120911
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name ESCITALOPRAM OXALATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Escitalopram


General Information