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Trazodone Hydrochloride - 60429-230-30 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 60429-230
Proprietary Name: Trazodone Hydrochloride
Non Proprietary Name: Trazodone Hydrochloride
Active Ingredient(s): 150    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: 60429-230
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071196
Marketing Category: ANDA
Start Marketing Date: 20081117

Package Information of Trazodone Hydrochloride

Package NDC: 60429-230-30
Package Description: 30 TABLET in 1 BOTTLE (60429-230-30)

NDC Information of Trazodone Hydrochloride

NDC Code 60429-230-30
Proprietary Name Trazodone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (60429-230-30)
Product NDC 60429-230
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 Golden State Medical Supply, Inc.
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


General Information