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Trazodone Hydrochloride - 68788-9861-9 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 68788-9861
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: 68788-9861
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of Trazodone Hydrochloride

Package NDC: 68788-9861-9
Package Description: 90 TABLET in 1 BOTTLE (68788-9861-9)

NDC Information of Trazodone Hydrochloride

NDC Code 68788-9861-9
Proprietary Name Trazodone Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (68788-9861-9)
Product NDC 68788-9861
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


General Information