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citalopram hydrobromide - 63629-3317-1 - (citalopram hydrobromide)

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Drug Information of citalopram hydrobromide

Product NDC: 63629-3317
Proprietary Name: citalopram hydrobromide
Non Proprietary Name: citalopram hydrobromide
Active Ingredient(s): 40    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: 63629-3317
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077032
Marketing Category: ANDA
Start Marketing Date: 20041112

Package Information of citalopram hydrobromide

Package NDC: 63629-3317-1
Package Description: 30 TABLET in 1 BOTTLE (63629-3317-1)

NDC Information of citalopram hydrobromide

NDC Code 63629-3317-1
Proprietary Name citalopram hydrobromide
Package Description 30 TABLET in 1 BOTTLE (63629-3317-1)
Product NDC 63629-3317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041112
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of citalopram hydrobromide


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