Citalopram - 0093-4742-01 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 0093-4742
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: 0093-4742
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077048
Marketing Category: ANDA
Start Marketing Date: 20071108

Package Information of Citalopram

Package NDC: 0093-4742-01
Package Description: 100 TABLET in 1 BOTTLE (0093-4742-01)

NDC Information of Citalopram

NDC Code 0093-4742-01
Proprietary Name Citalopram
Package Description 100 TABLET in 1 BOTTLE (0093-4742-01)
Product NDC 0093-4742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071108
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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