Citalopram - 43063-385-30 - (Citalopram)

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Drug Information of Citalopram

Product NDC: 43063-385
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: 43063-385
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077289
Marketing Category: ANDA
Start Marketing Date: 20100913

Package Information of Citalopram

Package NDC: 43063-385-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-385-30)

NDC Information of Citalopram

NDC Code 43063-385-30
Proprietary Name Citalopram
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-385-30)
Product NDC 43063-385
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100913
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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