Citalopram - 42806-021-30 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 42806-021
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 40    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 42806-021
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077045
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Citalopram

Package NDC: 42806-021-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)

NDC Information of Citalopram

NDC Code 42806-021-30
Proprietary Name Citalopram
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (42806-021-30)
Product NDC 42806-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information