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Trazodone Hydrochloride - 53489-517-07 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 53489-517
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trazodone Hydrochloride

Product NDC: 53489-517
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073137
Marketing Category: ANDA
Start Marketing Date: 19930324

Package Information of Trazodone Hydrochloride

Package NDC: 53489-517-07
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-07)

NDC Information of Trazodone Hydrochloride

NDC Code 53489-517-07
Proprietary Name Trazodone Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-07)
Product NDC 53489-517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19930324
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


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