Citalopram - 68084-580-01 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 68084-580
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: 68084-580
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20120730

Package Information of Citalopram

Package NDC: 68084-580-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-580-01) > 10 TABLET in 1 BLISTER PACK (68084-580-11)

NDC Information of Citalopram

NDC Code 68084-580-01
Proprietary Name Citalopram
Package Description 10 BLISTER PACK in 1 CARTON (68084-580-01) > 10 TABLET in 1 BLISTER PACK (68084-580-11)
Product NDC 68084-580
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120730
Marketing Category Name ANDA
Labeler Name American Health Packaging
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