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Nefazodone Hydrochloride - 49349-292-02 - (Nefazodone Hydrochloride)

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Drug Information of Nefazodone Hydrochloride

Product NDC: 49349-292
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: 49349-292
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076037
Marketing Category: ANDA
Start Marketing Date: 20110608

Package Information of Nefazodone Hydrochloride

Package NDC: 49349-292-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-292-02)

NDC Information of Nefazodone Hydrochloride

NDC Code 49349-292-02
Proprietary Name Nefazodone Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-292-02)
Product NDC 49349-292
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nefazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110608
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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