Citalopram - 67046-109-30 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 67046-109
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: 67046-109
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077289
Marketing Category: ANDA
Start Marketing Date: 20100630

Package Information of Citalopram

Package NDC: 67046-109-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-109-30)

NDC Information of Citalopram

NDC Code 67046-109-30
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BLISTER PACK (67046-109-30)
Product NDC 67046-109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100630
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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