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Citalopram Hydrobromide - 54458-922-05 - (Citalopram Hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 54458-922
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
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram Hydrobromide

Product NDC: 54458-922
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078216
Marketing Category: ANDA
Start Marketing Date: 20111007

Package Information of Citalopram Hydrobromide

Package NDC: 54458-922-05
Package Description: 360 TABLET in 1 CARTON (54458-922-05)

NDC Information of Citalopram Hydrobromide

NDC Code 54458-922-05
Proprietary Name Citalopram Hydrobromide
Package Description 360 TABLET in 1 CARTON (54458-922-05)
Product NDC 54458-922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111007
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
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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