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Trazodone Hydrochloride - 0603-6160-32 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 0603-6160
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trazodone Hydrochloride

Product NDC: 0603-6160
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072192
Marketing Category: ANDA
Start Marketing Date: 20100530

Package Information of Trazodone Hydrochloride

Package NDC: 0603-6160-32
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-6160-32)

NDC Information of Trazodone Hydrochloride

NDC Code 0603-6160-32
Proprietary Name Trazodone Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-6160-32)
Product NDC 0603-6160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100530
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
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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