TRAZODONE - 55289-223-90 - (TRAZODONE HYDROCHLORIDE)

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Drug Information of TRAZODONE

Product NDC: 55289-223
Proprietary Name: TRAZODONE
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

Product NDC: 55289-223
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071524
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of TRAZODONE

Package NDC: 55289-223-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (55289-223-90)

NDC Information of TRAZODONE

NDC Code 55289-223-90
Proprietary Name TRAZODONE
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (55289-223-90)
Product NDC 55289-223
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 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of TRAZODONE


General Information