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Trazodone Hydrochloride - 60505-2659-5 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 60505-2659
Proprietary Name: Trazodone Hydrochloride
Non Proprietary Name: Trazodone Hydrochloride
Active Ingredient(s): 300    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: 60505-2659
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071196
Marketing Category: ANDA
Start Marketing Date: 20090105

Package Information of Trazodone Hydrochloride

Package NDC: 60505-2659-5
Package Description: 500 TABLET in 1 BOTTLE (60505-2659-5)

NDC Information of Trazodone Hydrochloride

NDC Code 60505-2659-5
Proprietary Name Trazodone Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (60505-2659-5)
Product NDC 60505-2659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090105
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


General Information