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Trazodone Hydrochloride - 24236-624-30 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 24236-624
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: 24236-624
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071523
Marketing Category: ANDA
Start Marketing Date: 20130327

Package Information of Trazodone Hydrochloride

Package NDC: 24236-624-30
Package Description: 400 TABLET in 1 CANISTER (24236-624-30)

NDC Information of Trazodone Hydrochloride

NDC Code 24236-624-30
Proprietary Name Trazodone Hydrochloride
Package Description 400 TABLET in 1 CANISTER (24236-624-30)
Product NDC 24236-624
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130327
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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