NDC 15631-0599

HYDRASTIS CANADENSIS

Hydrastis Canadensis

HYDRASTIS CANADENSIS 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 Goldenseal.

Product ID15631-0599_c2082b04-46f9-4dfa-a2e5-8f71806c97b6
NDC15631-0599
Product TypeHuman Otc Drug
Proprietary NameHYDRASTIS CANADENSIS
Generic NameHydrastis Canadensis
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGOLDENSEAL
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0599-0

1 TABLET in 1 BLISTER PACK (15631-0599-0)
Marketing Start Date2016-01-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0599-4 [15631059904]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-2 [15631059902]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-6 [15631059906]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-0 [15631059900]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-1 [15631059901]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-5 [15631059905]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-3 [15631059903]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

NDC 15631-0599-7 [15631059907]

HYDRASTIS CANADENSIS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-01-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
GOLDENSEAL1 [hp_X]/1

OpenFDA Data

SPL SET ID:822007fc-566d-4794-bf98-4baee9c2faa2
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "HYDRASTIS CANADENSIS" or generic name "Hydrastis Canadensis"

    NDCBrand NameGeneric Name
    0220-2522Hydrastis canadensisGOLDENSEAL
    0220-2554Hydrastis canadensisGOLDENSEAL
    0220-2555Hydrastis canadensisGOLDENSEAL
    0220-2556Hydrastis canadensisGOLDENSEAL
    0220-2557Hydrastis canadensisGOLDENSEAL
    0220-2558Hydrastis canadensisGOLDENSEAL
    0220-2559Hydrastis canadensisGOLDENSEAL
    15631-0226HYDRASTIS CANADENSISHYDRASTIS CANADENSIS
    15631-0599HYDRASTIS CANADENSISHYDRASTIS CANADENSIS
    37662-1665Hydrastis CanadensisHydrastis Canadensis
    37662-1666Hydrastis CanadensisHydrastis Canadensis
    37662-1667Hydrastis CanadensisHydrastis Canadensis
    37662-1668Hydrastis CanadensisHydrastis Canadensis
    37662-1669Hydrastis CanadensisHydrastis Canadensis
    37662-1670Hydrastis CanadensisHydrastis Canadensis
    37662-1671Hydrastis CanadensisHydrastis Canadensis
    37662-1672Hydrastis CanadensisHydrastis Canadensis
    62106-8181HYDRASTIS CANADENSISGolden seal
    68428-428Hydrastis canadensisGOLDENSEAL
    71919-348Hydrastis canadensisGOLDENSEAL
    71919-763Hydrastis canadensisGOLDENSEAL
    71919-768Hydrastis canadensisGOLDENSEAL
    76472-1146HYDRASTIS CANADENSISGOLDENSEAL
    76472-3018HYDRASTIS CANADENSISHYDRASTIS CANADENSIS
    69152-1554Hydrastis canadensis 1XHydrastis canadensis
    69152-1102Hydrastis canadensis 200CHydrastis canadensis

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