Citalopram - 0615-6512-39 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 0615-6512
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: 0615-6512
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077048
Marketing Category: ANDA
Start Marketing Date: 20111207

Package Information of Citalopram

Package NDC: 0615-6512-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-6512-39)

NDC Information of Citalopram

NDC Code 0615-6512-39
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BLISTER PACK (0615-6512-39)
Product NDC 0615-6512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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