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Citalopram Hydrobromide - 55111-343-05 - (Citalopram Hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 55111-343
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: 55111-343
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077038
Marketing Category: ANDA
Start Marketing Date: 20041028

Package Information of Citalopram Hydrobromide

Package NDC: 55111-343-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (55111-343-05)

NDC Information of Citalopram Hydrobromide

NDC Code 55111-343-05
Proprietary Name Citalopram Hydrobromide
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (55111-343-05)
Product NDC 55111-343
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20041028
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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


General Information