Citalopram - 60505-2520-8 - (citalopram hydrobromide)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 60505-2520
Proprietary Name: Citalopram
Non Proprietary Name: citalopram hydrobromide
Active Ingredient(s): 40    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: 60505-2520
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077046
Marketing Category: ANDA
Start Marketing Date: 20110801

Package Information of Citalopram

Package NDC: 60505-2520-8
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2520-8)

NDC Information of Citalopram

NDC Code 60505-2520-8
Proprietary Name Citalopram
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2520-8)
Product NDC 60505-2520
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110801
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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