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Citalopram Hydrobromide - 55154-6660-0 - (citalopram hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 55154-6660
Proprietary Name: Citalopram Hydrobromide
Non Proprietary Name: citalopram hydrobromide
Active Ingredient(s): 20    mg/1 & nbsp;   citalopram hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram Hydrobromide

Product NDC: 55154-6660
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077046
Marketing Category: ANDA
Start Marketing Date: 20041124

Package Information of Citalopram Hydrobromide

Package NDC: 55154-6660-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-6660-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Citalopram Hydrobromide

NDC Code 55154-6660-0
Proprietary Name Citalopram Hydrobromide
Package Description 10 BLISTER PACK in 1 BAG (55154-6660-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-6660
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041124
Marketing Category Name ANDA
Labeler Name Cardinal Health
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 Hydrobromide


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