NDC 15631-0448

URANIUM NITRICUM

Uranium Nitricum

URANIUM NITRICUM 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 Uranyl Nitrate Hexahydrate.

Product ID15631-0448_586f13ce-6f94-4825-9d6e-e2d105b08848
NDC15631-0448
Product TypeHuman Otc Drug
Proprietary NameURANIUM NITRICUM
Generic NameUranium Nitricum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-02
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 15631-0448-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0448-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0448-2 [15631044802]

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

NDC 15631-0448-5 [15631044805]

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

NDC 15631-0448-3 [15631044803]

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

NDC 15631-0448-1 [15631044801]

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

NDC 15631-0448-0 [15631044800]

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

NDC 15631-0448-4 [15631044804]

URANIUM NITRICUM 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
URANYL NITRATE HEXAHYDRATE8 [hp_X]/1

OpenFDA Data

SPL SET ID:943e06bb-8c07-41f3-b450-cfea34940d71
Manufacturer
UNII

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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