NDC 15631-0417

STRAMONIUM

Stramonium

STRAMONIUM is a Oral Pellet 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 ID15631-0417_2519bc24-e468-4e69-a8c2-4d1693896a82
NDC15631-0417
Product TypeHuman Otc Drug
Proprietary NameSTRAMONIUM
Generic NameStramonium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-03
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 15631-0417-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0417-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0417-0 [15631041700]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0417-4 [15631041704]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0417-5 [15631041705]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0417-3 [15631041703]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0417-1 [15631041701]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0417-2 [15631041702]

STRAMONIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
DATURA STRAMONIUM6 [hp_X]/1

OpenFDA Data

SPL SET ID:754229d9-2aa4-43a8-a86f-facd7557fd97
Manufacturer
UNII

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

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