NDC 15631-0130

CHIONANTHUS VIRGINICA

Chionanthus Virginica

CHIONANTHUS VIRGINICA 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 Chionanthus Virginicus Bark.

Product ID15631-0130_065459ea-76b3-40bb-a05f-e3c4bb2874e8
NDC15631-0130
Product TypeHuman Otc Drug
Proprietary NameCHIONANTHUS VIRGINICA
Generic NameChionanthus Virginica
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 NameCHIONANTHUS VIRGINICUS BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0130-0

100 PELLET in 1 PACKAGE (15631-0130-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0130-0 [15631013000]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0130-2 [15631013002]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0130-4 [15631013004]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0130-5 [15631013005]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0130-1 [15631013001]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0130-3 [15631013003]

CHIONANTHUS VIRGINICA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

Drug Details

Active Ingredients

IngredientStrength
CHIONANTHUS VIRGINICUS BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:0e41fac2-49f6-48fb-8c0d-c37c56622f6d
Manufacturer
UNII

NDC Crossover Matching brand name "CHIONANTHUS VIRGINICA" or generic name "Chionanthus Virginica"

NDCBrand NameGeneric Name
0220-1329Chionanthus virginicaCHIONANTHUS VIRGINICUS BARK
15631-0130CHIONANTHUS VIRGINICACHIONANTHUS VIRGINICA
68428-311Chionanthus virginicaCHIONANTHUS VIRGINICUS BARK
71919-190Chionanthus virginicaCHIONANTHUS VIRGINICUS BARK

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