Citalopram - 0378-6233-01 - (citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 0378-6233
Proprietary Name: Citalopram
Non Proprietary Name: citalopram
Active Ingredient(s): 40    mg/1 & nbsp;   citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 0378-6233
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077042
Marketing Category: ANDA
Start Marketing Date: 20130208

Package Information of Citalopram

Package NDC: 0378-6233-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-01)

NDC Information of Citalopram

NDC Code 0378-6233-01
Proprietary Name Citalopram
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6233-01)
Product NDC 0378-6233
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130208
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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