NDC 15631-0698

THIOSINAMINUM

Thiosinaminum

THIOSINAMINUM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Allylthiourea.

Product ID15631-0698_e22a9c2d-bf6d-43b2-85a8-33c6d1aa7fe6
NDC15631-0698
Product TypeHuman Otc Drug
Proprietary NameTHIOSINAMINUM
Generic NameThiosinaminum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameALLYLTHIOUREA
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0698-7

10000 TABLET in 1 CONTAINER (15631-0698-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0698-3 [15631069803]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-6 [15631069806]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-4 [15631069804]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-5 [15631069805]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-1 [15631069801]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-7 [15631069807]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-0 [15631069800]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0698-2 [15631069802]

THIOSINAMINUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ALLYLTHIOUREA3 [hp_X]/1

OpenFDA Data

SPL SET ID:21c7262c-175f-4558-b849-f8146707552a
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "THIOSINAMINUM" or generic name "Thiosinaminum"

    NDCBrand NameGeneric Name
    0220-4971ThiosinaminumALLYLTHIOUREA
    0220-4972ThiosinaminumALLYLTHIOUREA
    0220-4979ThiosinaminumALLYLTHIOUREA
    0220-4980ThiosinaminumALLYLTHIOUREA
    0220-4983ThiosinaminumALLYLTHIOUREA
    0220-4984ThiosinaminumALLYLTHIOUREA
    15631-0440THIOSINAMINUMTHIOSINAMINUM
    15631-0698THIOSINAMINUMTHIOSINAMINUM
    15631-2323THIOSINAMINUMTHIOSINAMINUM
    37662-2305ThiosinaminumThiosinaminum
    37662-2306ThiosinaminumThiosinaminum
    37662-2307ThiosinaminumThiosinaminum
    37662-2308ThiosinaminumThiosinaminum
    37662-2309ThiosinaminumThiosinaminum
    37662-2310ThiosinaminumThiosinaminum
    37662-2311ThiosinaminumThiosinaminum
    37662-2312ThiosinaminumThiosinaminum
    62106-6482THIOSINAMINUMThiosinamine
    68428-674ThiosinaminumALLYLTHIOUREA
    71919-675THIOSINAMINUMAllylthiourea
    68428-721Be gone ScarsTHIOSINAMINUM

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