NDC 15631-0464

WYETHIA HELENIOIDES

Wyethia Helenioides

WYETHIA HELENIOIDES 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 Wyethia Helenioides Root.

Product ID15631-0464_342abbfa-587f-48ae-b4c9-0c1b81a62e44
NDC15631-0464
Product TypeHuman Otc Drug
Proprietary NameWYETHIA HELENIOIDES
Generic NameWyethia Helenioides
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameWYETHIA HELENIOIDES ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0464-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0464-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0464-5 [15631046405]

WYETHIA HELENIOIDES PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-11-01
Marketing End Date2020-03-27
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0464-4 [15631046404]

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

NDC 15631-0464-3 [15631046403]

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

NDC 15631-0464-0 [15631046400]

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

NDC 15631-0464-2 [15631046402]

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

NDC 15631-0464-1 [15631046401]

WYETHIA HELENIOIDES 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
WYETHIA HELENIOIDES ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:1939aa1f-c7ea-4d24-9626-413d3bfc58bc
Manufacturer
UNII

NDC Crossover Matching brand name "WYETHIA HELENIOIDES" or generic name "Wyethia Helenioides"

NDCBrand NameGeneric Name
0220-5307Wyethia helenioidesWYETHIA HELENIOIDES ROOT
0220-5308WYETHIA HELENIOIDESWYETHIA HELENIOIDES ROOT
15631-0464WYETHIA HELENIOIDESWYETHIA HELENIOIDES
68428-708Wyethia helenioidesWYETHIA HELENIOIDES ROOT
71919-719WYETHIA HELENIOIDESWYETHIA HELENIOIDES

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