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NEFAZODONE HYDROCHLORIDE - 16590-166-30 - (NEFAZODONE HYDROCHLORIDE)

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Drug Information of NEFAZODONE HYDROCHLORIDE

Product NDC: 16590-166
Proprietary Name: NEFAZODONE HYDROCHLORIDE
Non Proprietary Name: NEFAZODONE HYDROCHLORIDE
Active Ingredient(s): 100    mg/1 & nbsp;   NEFAZODONE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of NEFAZODONE HYDROCHLORIDE

Product NDC: 16590-166
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076037
Marketing Category: ANDA
Start Marketing Date: 20100818

Package Information of NEFAZODONE HYDROCHLORIDE

Package NDC: 16590-166-30
Package Description: 30 TABLET in 1 BOTTLE (16590-166-30)

NDC Information of NEFAZODONE HYDROCHLORIDE

NDC Code 16590-166-30
Proprietary Name NEFAZODONE HYDROCHLORIDE
Package Description 30 TABLET in 1 BOTTLE (16590-166-30)
Product NDC 16590-166
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NEFAZODONE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100818
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name NEFAZODONE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of NEFAZODONE HYDROCHLORIDE


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