Citalopram - 68788-0005-3 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 68788-0005
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 20    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 68788-0005
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077032
Marketing Category: ANDA
Start Marketing Date: 20110209

Package Information of Citalopram

Package NDC: 68788-0005-3
Package Description: 30 TABLET in 1 BOTTLE, DISPENSING (68788-0005-3)

NDC Information of Citalopram

NDC Code 68788-0005-3
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BOTTLE, DISPENSING (68788-0005-3)
Product NDC 68788-0005
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110209
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information