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Citalopram Hydrobromide - 53808-0351-1 - (CITALOPRAM HYDROBROMIDE)

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Drug Information of Citalopram Hydrobromide

Product NDC: 53808-0351
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: 53808-0351
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077046
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Citalopram Hydrobromide

Package NDC: 53808-0351-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0351-1)

NDC Information of Citalopram Hydrobromide

NDC Code 53808-0351-1
Proprietary Name Citalopram Hydrobromide
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0351-1)
Product NDC 53808-0351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CITALOPRAM HYDROBROMIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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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