Citalopram - 49349-731-30 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 49349-731
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 40    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 49349-731
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20130304

Package Information of Citalopram

Package NDC: 49349-731-30
Package Description: 400 TABLET in 1 CANISTER (49349-731-30)

NDC Information of Citalopram

NDC Code 49349-731-30
Proprietary Name Citalopram
Package Description 400 TABLET in 1 CANISTER (49349-731-30)
Product NDC 49349-731
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130304
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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