Citalopram - 54868-5178-1 - (Citalopram Hydrobromide)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 54868-5178
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram Hydrobromide
Active Ingredient(s): 20    mg/1 & nbsp;   Citalopram Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 54868-5178
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20080118

Package Information of Citalopram

Package NDC: 54868-5178-1
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE (54868-5178-1)

NDC Information of Citalopram

NDC Code 54868-5178-1
Proprietary Name Citalopram
Package Description 15 TABLET, FILM COATED in 1 BOTTLE (54868-5178-1)
Product NDC 54868-5178
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080118
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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