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Citalopram Hydrobromide - 68788-0802-3 - (Citalopram Hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 68788-0802
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: 68788-0802
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078216
Marketing Category: ANDA
Start Marketing Date: 20130326

Package Information of Citalopram Hydrobromide

Package NDC: 68788-0802-3
Package Description: 30 TABLET in 1 BOTTLE (68788-0802-3)

NDC Information of Citalopram Hydrobromide

NDC Code 68788-0802-3
Proprietary Name Citalopram Hydrobromide
Package Description 30 TABLET in 1 BOTTLE (68788-0802-3)
Product NDC 68788-0802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130326
Marketing Category Name ANDA
Labeler Name Preferred 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


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