NDC 15631-0168

DIOSCOREA VILLOSA

Dioscorea Villosa

DIOSCOREA VILLOSA 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 Dioscorea Villosa Tuber.

Product ID15631-0168_69166991-9ec7-4644-b9fd-c25705efa165
NDC15631-0168
Product TypeHuman Otc Drug
Proprietary NameDIOSCOREA VILLOSA
Generic NameDioscorea Villosa
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameDIOSCOREA VILLOSA TUBER
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0168-0

100 PELLET in 1 PACKAGE (15631-0168-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0168-4 [15631016804]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0168-2 [15631016802]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0168-1 [15631016801]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0168-0 [15631016800]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0168-3 [15631016803]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

NDC 15631-0168-5 [15631016805]

DIOSCOREA VILLOSA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-17

Drug Details

Active Ingredients

IngredientStrength
DIOSCOREA VILLOSA TUBER1 [hp_X]/1

OpenFDA Data

SPL SET ID:c08cfc8b-cc16-49d6-911c-94f2bd98db24
Manufacturer
UNII

NDC Crossover Matching brand name "DIOSCOREA VILLOSA" or generic name "Dioscorea Villosa"

NDCBrand NameGeneric Name
0220-1773Dioscorea villosaDIOSCOREA VILLOSA TUBER
0220-1775Dioscorea villosaDIOSCOREA VILLOSA TUBER
15631-0168DIOSCOREA VILLOSADIOSCOREA VILLOSA
15631-0574DIOSCOREA VILLOSADIOSCOREA VILLOSA
37662-0626Dioscorea VillosaDioscorea Villosa
37662-0627Dioscorea VillosaDioscorea Villosa
37662-0628Dioscorea VillosaDioscorea Villosa
37662-0629Dioscorea VillosaDioscorea Villosa
37662-0630Dioscorea VillosaDioscorea Villosa
37662-0631Dioscorea VillosaDioscorea Villosa
37662-0632Dioscorea VillosaDioscorea Villosa
37662-0633Dioscorea VillosaDioscorea Villosa
60512-6644DIOSCOREA VILLOSADIOSCOREA VILLOSA
68428-358Dioscorea villosaDIOSCOREA VILLOSA TUBER
71919-257Dioscorea villosaDIOSCOREA VILLOSA TUBER

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