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Nefazodone Hydrochloride - 21695-176-30 - (Nefazodone Hydrochloride)

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Drug Information of Nefazodone Hydrochloride

Product NDC: 21695-176
Proprietary Name: Nefazodone Hydrochloride
Non Proprietary Name: Nefazodone Hydrochloride
Active Ingredient(s): 200    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: 21695-176
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076037
Marketing Category: ANDA
Start Marketing Date: 20030916

Package Information of Nefazodone Hydrochloride

Package NDC: 21695-176-30
Package Description: 30 TABLET in 1 BOTTLE (21695-176-30)

NDC Information of Nefazodone Hydrochloride

NDC Code 21695-176-30
Proprietary Name Nefazodone Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (21695-176-30)
Product NDC 21695-176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nefazodone Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030916
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name NEFAZODONE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC]

Complete Information of Nefazodone Hydrochloride


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