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Trazodone Hydrochloride - 0904-3991-61 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 0904-3991
Proprietary Name: Trazodone Hydrochloride
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 Hydrochloride

Product NDC: 0904-3991
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071524
Marketing Category: ANDA
Start Marketing Date: 20040203

Package Information of Trazodone Hydrochloride

Package NDC: 0904-3991-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-3991-61)

NDC Information of Trazodone Hydrochloride

NDC Code 0904-3991-61
Proprietary Name Trazodone Hydrochloride
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-3991-61)
Product NDC 0904-3991
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 Major Pharmaceuticals
Substance Name TRAZODONE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Trazodone Hydrochloride


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