NDC 15631-0538

BERBERIS AQUIFOLIUM

Berberis Aquifolium

BERBERIS AQUIFOLIUM is a Oral Tablet 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 ID15631-0538_31ac8c9d-9b75-4ae8-9fa3-f2af27dc6afc
NDC15631-0538
Product TypeHuman Otc Drug
Proprietary NameBERBERIS AQUIFOLIUM
Generic NameBerberis Aquifolium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-30
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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0538-0

1 TABLET in 1 BLISTER PACK (15631-0538-0)
Marketing Start Date2015-12-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0538-6 [15631053806]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-0 [15631053800]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-7 [15631053807]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-5 [15631053805]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-3 [15631053803]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-4 [15631053804]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-2 [15631053802]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

NDC 15631-0538-1 [15631053801]

BERBERIS AQUIFOLIUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-30
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MAHONIA AQUIFOLIUM ROOT BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:685f7285-8449-4810-ad28-e7c8b2f13cb2
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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