NDC 68788-7246

Nefazodone Hydrochloride

Nefazodone Hydrochloride

Nefazodone Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is Nefazodone Hydrochloride.

Product ID68788-7246_23a5ef14-e507-404b-811f-090b903a3ba8
NDC68788-7246
Product TypeHuman Prescription Drug
Proprietary NameNefazodone Hydrochloride
Generic NameNefazodone Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-08-20
Marketing CategoryANDA / ANDA
Application NumberANDA076037
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameNEFAZODONE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68788-7246-1

100 TABLET in 1 BOTTLE (68788-7246-1)
Marketing Start Date2018-08-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7246-1 [68788724601]

Nefazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076037
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-20

NDC 68788-7246-9 [68788724609]

Nefazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076037
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-20

NDC 68788-7246-6 [68788724606]

Nefazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076037
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-20

NDC 68788-7246-8 [68788724608]

Nefazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076037
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-20

NDC 68788-7246-3 [68788724603]

Nefazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA076037
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-08-20

Drug Details

Active Ingredients

IngredientStrength
NEFAZODONE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:fa83c4e0-00b2-4203-847f-38a3d820e843
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1098666

    • Pharmacological Class

    • Serotonin Reuptake Inhibitor [EPC]

    NDC Crossover Matching brand name "Nefazodone Hydrochloride" or generic name "Nefazodone Hydrochloride"

    NDCBrand NameGeneric Name
    0093-1024Nefazodone HydrochlorideNefazodone Hydrochloride
    0093-1025Nefazodone HydrochlorideNefazodone Hydrochloride
    0093-1026Nefazodone HydrochlorideNefazodone Hydrochloride
    0093-7113Nefazodone HydrochlorideNefazodone Hydrochloride
    0093-7178Nefazodone HydrochlorideNefazodone Hydrochloride
    21695-174Nefazodone HydrochlorideNefazodone Hydrochloride
    21695-175Nefazodone HydrochlorideNefazodone Hydrochloride
    21695-176Nefazodone HydrochlorideNefazodone Hydrochloride
    21695-177Nefazodone HydrochlorideNefazodone Hydrochloride
    63629-7046Nefazodone HydrochlorideNefazodone Hydrochloride
    63629-7214Nefazodone HydrochlorideNefazodone Hydrochloride
    63629-7310Nefazodone HydrochlorideNefazodone Hydrochloride
    68788-7217Nefazodone HydrochlorideNefazodone Hydrochloride
    68788-7242Nefazodone HydrochlorideNefazodone Hydrochloride
    68788-7246Nefazodone HydrochlorideNefazodone Hydrochloride
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