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Trazodone Hydrochloride - 21695-133-72 - (Trazodone)

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Drug Information of Trazodone Hydrochloride

Product NDC: 21695-133
Proprietary Name: Trazodone Hydrochloride
Non Proprietary Name: Trazodone
Active Ingredient(s): 50    mg/1 & nbsp;   Trazodone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Trazodone Hydrochloride

Product NDC: 21695-133
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 19871211

Package Information of Trazodone Hydrochloride

Package NDC: 21695-133-72
Package Description: 120 TABLET in 1 BOTTLE (21695-133-72)

NDC Information of Trazodone Hydrochloride

NDC Code 21695-133-72
Proprietary Name Trazodone Hydrochloride
Package Description 120 TABLET in 1 BOTTLE (21695-133-72)
Product NDC 21695-133
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871211
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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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