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Trazodone Hydrochloride - 55289-060-14 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 55289-060
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
Coding System: National Drug Codes(NDC)

Labeler Information of Trazodone Hydrochloride

Product NDC: 55289-060
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071525
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Trazodone Hydrochloride

Package NDC: 55289-060-14
Package Description: 14 TABLET in 1 BOTTLE, PLASTIC (55289-060-14)

NDC Information of Trazodone Hydrochloride

NDC Code 55289-060-14
Proprietary Name Trazodone Hydrochloride
Package Description 14 TABLET in 1 BOTTLE, PLASTIC (55289-060-14)
Product NDC 55289-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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