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CITALOPRAM HYDROBROMIDE - 76282-208-30 - (CITALOPRAM)

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Drug Information of CITALOPRAM HYDROBROMIDE

Product NDC: 76282-208
Proprietary Name: CITALOPRAM HYDROBROMIDE
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 HYDROBROMIDE

Product NDC: 76282-208
Labeler Name: Exelan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077534
Marketing Category: ANDA
Start Marketing Date: 20121001

Package Information of CITALOPRAM HYDROBROMIDE

Package NDC: 76282-208-30
Package Description: 30 TABLET in 1 BOTTLE (76282-208-30)

NDC Information of CITALOPRAM HYDROBROMIDE

NDC Code 76282-208-30
Proprietary Name CITALOPRAM HYDROBROMIDE
Package Description 30 TABLET in 1 BOTTLE (76282-208-30)
Product NDC 76282-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CITALOPRAM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121001
Marketing Category Name ANDA
Labeler Name Exelan 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 HYDROBROMIDE


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