Citalopram - 53808-0227-1 - (Citalopram Hydrobromide)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 53808-0227
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram Hydrobromide
Active Ingredient(s): 40    mg/1 & nbsp;   Citalopram Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 53808-0227
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Citalopram

Package NDC: 53808-0227-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0227-1)

NDC Information of Citalopram

NDC Code 53808-0227-1
Proprietary Name Citalopram
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0227-1)
Product NDC 53808-0227
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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