Citalopram - 65862-007-01 - (Citalopram Hydrobromide)

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Drug Information of Citalopram

Product NDC: 65862-007
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: 65862-007
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20041028

Package Information of Citalopram

Package NDC: 65862-007-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)

NDC Information of Citalopram

NDC Code 65862-007-01
Proprietary Name Citalopram
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (65862-007-01)
Product NDC 65862-007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041028
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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