NDC 15631-0238

IRIDIUM METALLICUM

Iridium Metallicum

IRIDIUM METALLICUM 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 Iridium.

Product ID15631-0238_a148eda4-6c01-1b54-e053-2a95a90a2b30
NDC15631-0238
Product TypeHuman Otc Drug
Proprietary NameIRIDIUM METALLICUM
Generic NameIridium Metallicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameIRIDIUM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0238-0

100 PELLET in 1 PACKAGE (15631-0238-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0238-5 [15631023805]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0238-2 [15631023802]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0238-1 [15631023801]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0238-3 [15631023803]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0238-4 [15631023804]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0238-0 [15631023800]

IRIDIUM METALLICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
IRIDIUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:b78ad6ad-4492-4808-b691-17f4b745de8f
Manufacturer
UNII

NDC Crossover Matching brand name "IRIDIUM METALLICUM" or generic name "Iridium Metallicum"

NDCBrand NameGeneric Name
15631-0238IRIDIUM METALLICUMIRIDIUM METALLICUM
37662-0851Iridium MetallicumIridium Metallicum
37662-0852Iridium MetallicumIridium Metallicum
37662-0853Iridium MetallicumIridium Metallicum
37662-0854Iridium MetallicumIridium Metallicum
37662-0855Iridium MetallicumIridium Metallicum
37662-0856Iridium MetallicumIridium Metallicum
37662-0857Iridium MetallicumIridium Metallicum
37662-0858Iridium MetallicumIridium Metallicum
68428-442Iridium metallicumIRIDIUM
71919-367Iridium metallicumIRIDIUM

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