NDC 10702-040

BENZPHETAMINE HYDROCHLORIDE

Benzphetamine Hydrochloride

BENZPHETAMINE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Kvk-tech, Inc. The primary component is Benzphetamine Hydrochloride.

Product ID10702-040_53fbe009-c089-4194-a4df-d3d0ed5cd058
NDC10702-040
Product TypeHuman Prescription Drug
Proprietary NameBENZPHETAMINE HYDROCHLORIDE
Generic NameBenzphetamine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-07-21
Marketing CategoryANDA / ANDA
Application NumberANDA090968
Labeler NameKVK-TECH, INC
Substance NameBENZPHETAMINE HYDROCHLORIDE
Active Ingredient Strength50 mg/1
Pharm ClassesAppetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
DEA ScheduleCIII
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 10702-040-01

100 TABLET in 1 BOTTLE (10702-040-01)
Marketing Start Date2010-07-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 10702-040-10 [10702004010]

BENZPHETAMINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA090968
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-07-21

NDC 10702-040-03 [10702004003]

BENZPHETAMINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA090968
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-07-21

NDC 10702-040-01 [10702004001]

BENZPHETAMINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA090968
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-07-21

NDC 10702-040-50 [10702004050]

BENZPHETAMINE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA090968
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-07-21

Drug Details

Active Ingredients

IngredientStrength
BENZPHETAMINE HYDROCHLORIDE50 mg/1

OpenFDA Data

SPL SET ID:14d4589d-7f1c-4b6e-9557-59dad39b0960
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 904368

    • Pharmacological Class

    • Appetite Suppression [PE]
    • Increased Sympathetic Activity [PE]
    • Sympathomimetic Amine Anorectic [EPC]
    • Appetite Suppression [PE]
    • Increased Sympathetic Activity [PE]
    • Sympathomimetic Amine Anorectic [EPC]

    Medicade Reported Pricing

    10702004050 BENZPHETAMINE HCL 50 MG TABLET

    Pricing Unit: EA | Drug Type:

    10702004003 BENZPHETAMINE HCL 50 MG TABLET

    Pricing Unit: EA | Drug Type:

    10702004001 BENZPHETAMINE HCL 50 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "BENZPHETAMINE HYDROCHLORIDE" or generic name "Benzphetamine Hydrochloride"

    NDCBrand NameGeneric Name
    10702-040BENZPHETAMINE HYDROCHLORIDEbenzphetamine hydrochloride
    12634-118Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    23155-174Benzphetamine HydrochlorideBenzphetamine Hydrochloride Tablets
    33261-458BENZPHETAMINE HYDROCHLORIDEbenzphetamine hydrochloride
    42806-081Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    43063-541BENZPHETAMINE HYDROCHLORIDEbenzphetamine hydrochloride
    43547-263benzphetamine hydrochloridebenzphetamine hydrochloride
    46672-843benzphetamine hydrochloridebenzphetamine hydrochloride
    46672-844benzphetamine hydrochloridebenzphetamine hydrochloride
    50090-1024BENZPHETAMINE HYDROCHLORIDEbenzphetamine hydrochloride
    50090-5837Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    53217-175Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    63629-4139Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    71335-0451BENZPHETAMINE HYDROCHLORIDEbenzphetamine hydrochloride
    71335-0768Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    75834-100Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    75834-102Benzphetamine HydrochlorideBenzphetamine Hydrochloride
    76519-1154BENZPHETAMINE HYDROCHLORIDEBENZPHETAMINE HYDROCHLORIDE
    66992-399Regimexbenzphetamine hydrochloride
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.