Citalopram - 60429-175-10 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 60429-175
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 40    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 60429-175
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077045
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Citalopram

Package NDC: 60429-175-10
Package Description: 1000 TABLET in 1 BOTTLE (60429-175-10)

NDC Information of Citalopram

NDC Code 60429-175-10
Proprietary Name Citalopram
Package Description 1000 TABLET in 1 BOTTLE (60429-175-10)
Product NDC 60429-175
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
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