NDC 15631-0691

STRAMONIUM

Stramonium

STRAMONIUM 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 Datura Stramonium.

Product ID15631-0691_a67885c3-4f68-496c-940d-f5759cdee394
NDC15631-0691
Product TypeHuman Otc Drug
Proprietary NameSTRAMONIUM
Generic NameStramonium
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 NameDATURA STRAMONIUM
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0691-3

100 TABLET in 1 CONTAINER (15631-0691-3)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0691-1 [15631069101]

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

NDC 15631-0691-7 [15631069107]

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

NDC 15631-0691-0 [15631069100]

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

NDC 15631-0691-2 [15631069102]

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

NDC 15631-0691-5 [15631069105]

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

NDC 15631-0691-6 [15631069106]

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

NDC 15631-0691-3 [15631069103]

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

NDC 15631-0691-4 [15631069104]

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

Drug Details

Active Ingredients

IngredientStrength
DATURA STRAMONIUM6 [hp_X]/1

OpenFDA Data

SPL SET ID:4e92fdb8-c457-49bd-b748-296b63b69165
Manufacturer
UNII
UPC Code
  • 8907460005526

    • NDC Crossover Matching brand name "STRAMONIUM" or generic name "Stramonium"

    NDCBrand NameGeneric Name
    0220-4752StramoniumDATURA STRAMONIUM
    0220-4753StramoniumDATURA STRAMONIUM
    0220-4760StramoniumDATURA STRAMONIUM
    0220-4761StramoniumDATURA STRAMONIUM
    0220-4768StramoniumDATURA STRAMONIUM
    0220-4771StramoniumDATURA STRAMONIUM
    0220-4772StramoniumDATURA STRAMONIUM
    0220-4773StramoniumDATURA STRAMONIUM
    0360-0362STRAMONIUMSTRAMONIUM
    0360-0363STRAMONIUMSTRAMONIUM
    15631-0417STRAMONIUMSTRAMONIUM
    15631-0691STRAMONIUMSTRAMONIUM
    37662-2165StramoniumStramonium
    37662-2166StramoniumStramonium
    37662-2167StramoniumStramonium
    37662-2168StramoniumStramonium
    37662-2169StramoniumStramonium
    37662-2170StramoniumStramonium
    37662-2171StramoniumStramonium
    37662-2172StramoniumStramonium
    44911-0393StramoniumStramonium
    53645-2040StramoniumStramonium
    62106-8982STRAMONIUMThorn apple
    68428-651StramoniumDATURA STRAMONIUM
    71919-648STRAMONIUMDatura stramonium
    69152-1171Stramonium 200CStramonium
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.