TRAZODONE - 55289-064-60 - (TRAZODONE HYDROCHLORIDE)

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Drug Information of TRAZODONE

Product NDC: 55289-064
Proprietary Name: TRAZODONE
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

Product NDC: 55289-064
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of TRAZODONE

Package NDC: 55289-064-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (55289-064-60)

NDC Information of TRAZODONE

NDC Code 55289-064-60
Proprietary Name TRAZODONE
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (55289-064-60)
Product NDC 55289-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TRAZODONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of TRAZODONE


General Information