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Trazodone Hydrochloride - 68387-166-30 - (Trazodone Hydrochloride)

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Drug Information of Trazodone Hydrochloride

Product NDC: 68387-166
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: 68387-166
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072193
Marketing Category: ANDA
Start Marketing Date: 20101117

Package Information of Trazodone Hydrochloride

Package NDC: 68387-166-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68387-166-30)

NDC Information of Trazodone Hydrochloride

NDC Code 68387-166-30
Proprietary Name Trazodone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68387-166-30)
Product NDC 68387-166
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101117
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
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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