Celexa - 54868-4985-0 - (citalopram hydrobromide)

Alphabetical Index


Drug Information of Celexa

Product NDC: 54868-4985
Proprietary Name: Celexa
Non Proprietary Name: citalopram hydrobromide
Active Ingredient(s): 10    mg/1 & nbsp;   citalopram hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Celexa

Product NDC: 54868-4985
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020822
Marketing Category: NDA
Start Marketing Date: 20040130

Package Information of Celexa

Package NDC: 54868-4985-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (54868-4985-0)

NDC Information of Celexa

NDC Code 54868-4985-0
Proprietary Name Celexa
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (54868-4985-0)
Product NDC 54868-4985
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040130
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Celexa


General Information