Citalopram - 60429-173-30 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 60429-173
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 10    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 60429-173
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: 60429-173-30
Package Description: 30 TABLET in 1 BOTTLE (60429-173-30)

NDC Information of Citalopram

NDC Code 60429-173-30
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BOTTLE (60429-173-30)
Product NDC 60429-173
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 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information