Citalopram - 55154-8267-9 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 55154-8267
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 20    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 55154-8267
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077048
Marketing Category: ANDA
Start Marketing Date: 20110119

Package Information of Citalopram

Package NDC: 55154-8267-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-8267-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Citalopram

NDC Code 55154-8267-9
Proprietary Name Citalopram
Package Description 6 BLISTER PACK in 1 CARTON (55154-8267-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-8267
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110119
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information