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Trazodone Hydrochloride - 54868-0122-6 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 54868-0122
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: 54868-0122
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 19960409

Package Information of Trazodone Hydrochloride

Package NDC: 54868-0122-6
Package Description: 100 TABLET in 1 BOTTLE, UNIT-DOSE (54868-0122-6)

NDC Information of Trazodone Hydrochloride

NDC Code 54868-0122-6
Proprietary Name Trazodone Hydrochloride
Package Description 100 TABLET in 1 BOTTLE, UNIT-DOSE (54868-0122-6)
Product NDC 54868-0122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960409
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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