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Trazodone Hydrochloride - 0615-2578-31 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 0615-2578
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: 0615-2578
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Trazodone Hydrochloride

Package NDC: 0615-2578-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-2578-31)

NDC Information of Trazodone Hydrochloride

NDC Code 0615-2578-31
Proprietary Name Trazodone Hydrochloride
Package Description 31 TABLET in 1 BLISTER PACK (0615-2578-31)
Product NDC 0615-2578
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


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