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ESCITALOPRAM - 42549-672-60 - (ESCITALOPRAM)

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Drug Information of ESCITALOPRAM

Product NDC: 42549-672
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: 42549-672
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076765
Marketing Category: ANDA
Start Marketing Date: 20120314

Package Information of ESCITALOPRAM

Package NDC: 42549-672-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (42549-672-60)

NDC Information of ESCITALOPRAM

NDC Code 42549-672-60
Proprietary Name ESCITALOPRAM
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (42549-672-60)
Product NDC 42549-672
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 STAT Rx USA LLC
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


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