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Trazodone Hydrochloride - 60505-2654-0 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 60505-2654
Proprietary Name: Trazodone Hydrochloride
Non Proprietary Name: Trazodone Hydrochloride
Active Ingredient(s): 100    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: 60505-2654
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071196
Marketing Category: ANDA
Start Marketing Date: 20081117

Package Information of Trazodone Hydrochloride

Package NDC: 60505-2654-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-2654-0) > 10 TABLET in 1 BLISTER PACK

NDC Information of Trazodone Hydrochloride

NDC Code 60505-2654-0
Proprietary Name Trazodone Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (60505-2654-0) > 10 TABLET in 1 BLISTER PACK
Product NDC 60505-2654
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 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


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