NDC 15631-0079

BERBERIS AQUIFOLIUM

Berberis Aquifolium

BERBERIS AQUIFOLIUM 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 Mahonia Aquifolium Root Bark.

Product ID15631-0079_9eca129f-e1ea-fdce-e053-2a95a90a4684
NDC15631-0079
Product TypeHuman Otc Drug
Proprietary NameBERBERIS AQUIFOLIUM
Generic NameBerberis Aquifolium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameMAHONIA AQUIFOLIUM ROOT BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0079-0

100 PELLET in 1 PACKAGE (15631-0079-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0079-3 [15631007903]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0079-0 [15631007900]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0079-5 [15631007905]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0079-2 [15631007902]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0079-4 [15631007904]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0079-1 [15631007901]

BERBERIS AQUIFOLIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

Drug Details

Active Ingredients

IngredientStrength
MAHONIA AQUIFOLIUM ROOT BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:644125fe-7098-43dd-b3fe-df82f217a249
Manufacturer
UNII

NDC Crossover Matching brand name "BERBERIS AQUIFOLIUM" or generic name "Berberis Aquifolium"

NDCBrand NameGeneric Name
0220-0831Berberis aquifoliumBERBERIS AQUIFOLIUM ROOT BARK
15631-0079BERBERIS AQUIFOLIUMBERBERIS AQUIFOLIUM
15631-0538BERBERIS AQUIFOLIUMBERBERIS AQUIFOLIUM
68428-256Berberis aquifoliumMAHONIA AQUIFOLIUM ROOT BARK
71919-119Berberis aquifoliumBERBERIS AQUIFOLIUM ROOT BARK

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