Citalopram - 24658-141-30 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 24658-141
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 20    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 24658-141
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077534
Marketing Category: ANDA
Start Marketing Date: 20070403

Package Information of Citalopram

Package NDC: 24658-141-30
Package Description: 30 TABLET in 1 BOTTLE (24658-141-30)

NDC Information of Citalopram

NDC Code 24658-141-30
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BOTTLE (24658-141-30)
Product NDC 24658-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070403
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, LLC
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information