NDC 15631-0459

VIBURNUM OPULUS

Viburnum Opulus

VIBURNUM OPULUS 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 Viburnum Opulus Bark.

Product ID15631-0459_a1d466f5-9370-7977-e053-2a95a90a05a0
NDC15631-0459
Product TypeHuman Otc Drug
Proprietary NameVIBURNUM OPULUS
Generic NameViburnum Opulus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameVIBURNUM OPULUS BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0459-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0459-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0459-4 [15631045904]

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

NDC 15631-0459-0 [15631045900]

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

NDC 15631-0459-1 [15631045901]

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

NDC 15631-0459-3 [15631045903]

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

NDC 15631-0459-5 [15631045905]

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

NDC 15631-0459-2 [15631045902]

VIBURNUM OPULUS 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
VIBURNUM OPULUS BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:d4001d63-d009-4374-8bd8-6cb4dab0eaec
Manufacturer
UNII

NDC Crossover Matching brand name "VIBURNUM OPULUS" or generic name "Viburnum Opulus"

NDCBrand NameGeneric Name
0220-5258Viburnum opulusVIBURNUM OPULUS BARK
0220-5259VIBURNUM OPULUSVIBURNUM OPULUS BARK
0220-5260VIBURNUM OPULUSVIBURNUM OPULUS BARK
15631-0459VIBURNUM OPULUSVIBURNUM OPULUS
37662-1341Viburnum OpulusViburnum Opulus
37662-1342Viburnum OpulusViburnum Opulus
37662-1343Viburnum OpulusViburnum Opulus
37662-1344Viburnum OpulusViburnum Opulus
37662-1345Viburnum OpulusViburnum Opulus
37662-1346Viburnum OpulusViburnum Opulus
37662-1347Viburnum OpulusViburnum Opulus
37662-1348Viburnum OpulusViburnum Opulus
68428-702Viburnum opulusVIBURNUM OPULUS BARK
71919-711VIBURNUM OPULUSViburnum opulus

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