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Trazodone Hydrochloride - 55154-0659-0 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 55154-0659
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: 55154-0659
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071524
Marketing Category: ANDA
Start Marketing Date: 20040203

Package Information of Trazodone Hydrochloride

Package NDC: 55154-0659-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0659-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Trazodone Hydrochloride

NDC Code 55154-0659-0
Proprietary Name Trazodone Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-0659-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0659
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040203
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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