NDC 72988-0016

INSADOL

Corn Sterilized Quantitative Extract (beta Sitosterol)

INSADOL is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Lydia Co., Ltd. The primary component is .beta.-sitosterol.

Product ID72988-0016_945bd5ac-088f-06f1-e053-2a95a90a33ff
NDC72988-0016
Product TypeHuman Otc Drug
Proprietary NameINSADOL
Generic NameCorn Sterilized Quantitative Extract (beta Sitosterol)
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-10-08
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameLYDIA Co., Ltd
Substance Name.BETA.-SITOSTEROL
Active Ingredient Strength35 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72988-0016-1

100 TABLET in 1 BLISTER PACK (72988-0016-1)
Marketing Start Date2019-10-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72988-0016-1 [72988001601]

INSADOL TABLET
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-08

Drug Details

Active Ingredients

IngredientStrength
.BETA.-SITOSTEROL35 mg/1

OpenFDA Data

SPL SET ID:945bd5ac-088d-06f1-e053-2a95a90a33ff
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 2104173
  • NDC Crossover Matching brand name "INSADOL" or generic name "Corn Sterilized Quantitative Extract (beta Sitosterol)"

    NDCBrand NameGeneric Name
    72689-0007INSADOLCorn sterilized quantitative extract (beta sitosterol)
    72988-0016INSADOLCorn sterilized quantitative extract (beta sitosterol)
    73442-0002INSADOLCorn sterilized quantitative extract (beta sitosterol)

    Trademark Results [INSADOL]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    INSADOL
    INSADOL
    97575733 not registered Live/Pending
    Kim, Anthony H.
    2022-09-01
    INSADOL
    INSADOL
    72229032 0813338 Dead/Expired
    SERDEX-SOCIETE D'ETUDES DE RECHERCHES DE DIFFUSION ET D'EXPLOITATION
    1965-09-30

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.