NDC 61502-922

PHENDIMETRAZINE TARTRATE

Phendimetrazine Tartrate

PHENDIMETRAZINE TARTRATE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Epm Packaging Inc. The primary component is Phendimetrazine Tartrate.

Product ID61502-922_2a52224e-60c6-6204-e054-00144ff8d46c
NDC61502-922
Product TypeHuman Prescription Drug
Proprietary NamePHENDIMETRAZINE TARTRATE
Generic NamePhendimetrazine Tartrate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-26
Marketing CategoryANDA / ANDA
Application NumberANDA091042
Labeler NameEPM Packaging Inc
Substance NamePHENDIMETRAZINE TARTRATE
Active Ingredient Strength35 mg/1
Pharm ClassesAppetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
DEA ScheduleCIII
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 61502-922-97

500 TABLET in 1 BOTTLE (61502-922-97)
Marketing Start Date2016-01-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 61502-922-96 [61502092296]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-30 [61502092230]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-20 [61502092220]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-15 [61502092215]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-97 [61502092297]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-06 [61502092206]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

NDC 61502-922-10 [61502092210]

PHENDIMETRAZINE TARTRATE TABLET
Marketing CategoryANDA
Application NumberANDA091042
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PHENDIMETRAZINE TARTRATE35 mg/1

OpenFDA Data

SPL SET ID:2a4310c1-f064-6df5-e054-00144ff88e88
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 979549
    • UPC Code
  • 0361502922307

    • Pharmacological Class

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

    NDC Crossover Matching brand name "PHENDIMETRAZINE TARTRATE" or generic name "Phendimetrazine Tartrate"

    NDCBrand NameGeneric Name
    0185-4057Phendimetrazine TartratePhendimetrazine Tartrate
    0185-5254Phendimetrazine TartratePhendimetrazine Tartrate
    0463-8000phendimetrazine tartratephendimetrazine tartrate
    0463-8500phendimetrazine tartratephendimetrazine tartrate
    10544-041Phendimetrazine TartratePhendimetrazine Tartrate
    10702-045Phendimetrazine TartratePhendimetrazine Tartrate
    10702-077Phendimetrazine TartratePhendimetrazine Tartrate
    10702-078Phendimetrazine TartratePhendimetrazine Tartrate
    12634-028phendimetrazine tartratephendimetrazine tartrate
    12634-539phendimetrazine tartratephendimetrazine tartrate
    12634-910Phendimetrazine TartratePhendimetrazine Tartrate
    17224-500Phendimetrazine TartratePhendimetrazine Tartrate
    17224-501PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    17224-831PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    21695-597Phendimetrazine TartratePhendimetrazine Tartrate
    33261-341Phendimetrazine TartratePhendimetrazine Tartrate
    33261-390Phendimetrazine TartratePhendimetrazine Tartrate
    43063-510Phendimetrazine TartratePhendimetrazine Tartrate
    43063-892PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    43547-264phendimetrazine tartratephendimetrazine tartrate
    46672-138phendimetrazine tartratephendimetrazine tartrate
    50090-0338Phendimetrazine TartratePhendimetrazine Tartrate
    50090-0715Phendimetrazine TartratePhendimetrazine Tartrate
    50090-2235Phendimetrazine TartratePhendimetrazine Tartrate
    50090-2592Phendimetrazine TartratePhendimetrazine Tartrate
    50090-3976Phendimetrazine TartratePhendimetrazine Tartrate
    50090-3988PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    68071-3062Phendimetrazine TartratePhendimetrazine Tartrate
    68071-3040Phendimetrazine TartratePhendimetrazine Tartrate
    68462-561PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    68788-9743Phendimetrazine TartratePhendimetrazine Tartrate
    68788-7236Phendimetrazine TartratePhendimetrazine Tartrate
    69543-409PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    69543-410PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    70518-1430Phendimetrazine TartratePhendimetrazine Tartrate
    71335-0110phendimetrazine tartratephendimetrazine tartrate
    71335-0074Phendimetrazine TartratePhendimetrazine Tartrate
    71335-0324Phendimetrazine TartratePhendimetrazine Tartrate
    75921-045Phendimetrazine TartratePhendimetrazine Tartrate
    52959-282Phendimetrazine TartratePhendimetrazine Tartrate
    61502-922PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    63187-898Phendimetrazine TartratePhendimetrazine Tartrate
    63629-7319phendimetrazine tartratephendimetrazine tartrate
    63629-1604Phendimetrazine TartratePhendimetrazine Tartrate
    63629-3051Phendimetrazine TartratePhendimetrazine Tartrate
    63629-7266Phendimetrazine TartratePhendimetrazine Tartrate
    64850-900Phendimetrazine TartratePhendimetrazine Tartrate
    64850-440PHENDIMETRAZINE TARTRATEPHENDIMETRAZINE TARTRATE
    66267-394Phendimetrazine TartratePhendimetrazine Tartrate
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.