Citalopram - 55154-6269-9 - (citalopram)

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Drug Information of Citalopram

Product NDC: 55154-6269
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: 55154-6269
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077042
Marketing Category: ANDA
Start Marketing Date: 20130208

Package Information of Citalopram

Package NDC: 55154-6269-9
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (55154-6269-9)

NDC Information of Citalopram

NDC Code 55154-6269-9
Proprietary Name Citalopram
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (55154-6269-9)
Product NDC 55154-6269
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130208
Marketing Category Name ANDA
Labeler Name Cardinal Health
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