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Trazodone Hydrochloride - 60505-2653-7 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 60505-2653
Proprietary Name: Trazodone Hydrochloride
Non Proprietary Name: Trazodone Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Trazodone Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trazodone Hydrochloride

Product NDC: 60505-2653
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071258
Marketing Category: ANDA
Start Marketing Date: 20081117

Package Information of Trazodone Hydrochloride

Package NDC: 60505-2653-7
Package Description: 17000 TABLET in 1 BOTTLE (60505-2653-7)

NDC Information of Trazodone Hydrochloride

NDC Code 60505-2653-7
Proprietary Name Trazodone Hydrochloride
Package Description 17000 TABLET in 1 BOTTLE (60505-2653-7)
Product NDC 60505-2653
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081117
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


General Information