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Trazodone Hydrochloride - 63629-3210-7 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 63629-3210
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: 63629-3210
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071524
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Trazodone Hydrochloride

Package NDC: 63629-3210-7
Package Description: 120 TABLET in 1 BOTTLE (63629-3210-7)

NDC Information of Trazodone Hydrochloride

NDC Code 63629-3210-7
Proprietary Name Trazodone Hydrochloride
Package Description 120 TABLET in 1 BOTTLE (63629-3210-7)
Product NDC 63629-3210
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 Bryant Ranch Prepack
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


General Information