NDC 15631-0700

URANIUM NITRICUM

Uranium Nitricum

URANIUM NITRICUM 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 Uranyl Nitrate Hexahydrate.

Product ID15631-0700_0958841b-8d8d-45c8-a6ad-540b59760ab6
NDC15631-0700
Product TypeHuman Otc Drug
Proprietary NameURANIUM NITRICUM
Generic NameUranium Nitricum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameURANYL NITRATE HEXAHYDRATE
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0700-7

10000 TABLET in 1 CONTAINER (15631-0700-7)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0700-7 [15631070007]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-4 [15631070004]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-1 [15631070001]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-6 [15631070006]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-2 [15631070002]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-0 [15631070000]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-5 [15631070005]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0700-3 [15631070003]

URANIUM NITRICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
URANYL NITRATE HEXAHYDRATE8 [hp_X]/1

OpenFDA Data

SPL SET ID:af37b43a-85ed-4bdd-b637-84d51dc1966c
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "URANIUM NITRICUM" or generic name "Uranium Nitricum"

    NDCBrand NameGeneric Name
    15631-0448URANIUM NITRICUMURANIUM NITRICUM
    15631-0700URANIUM NITRICUMURANIUM NITRICUM
    68428-687Uranium nitricumURANYL NITRATE HEXAHYDRATE
    71919-693URANIUM NITRICUMUranyl nitrate hexahydrate
    61657-0965Total UraniumUranium Nitricum

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