Home > National Drug Code (NDC) > Citalopram Hydrobromide

Citalopram Hydrobromide - 55289-883-60 - (Citalopram Hydrobromide)

Alphabetical Index


Drug Information of Citalopram Hydrobromide

Product NDC: 55289-883
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: 55289-883
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077032
Marketing Category: ANDA
Start Marketing Date: 20100510

Package Information of Citalopram Hydrobromide

Package NDC: 55289-883-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-883-60)

NDC Information of Citalopram Hydrobromide

NDC Code 55289-883-60
Proprietary Name Citalopram Hydrobromide
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-883-60)
Product NDC 55289-883
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100510
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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


General Information