NDC 15631-0433

TELLURIUM METALLICUM

Tellurium Metallicum

TELLURIUM 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 Tellurium.

Product ID15631-0433_a1d0c4df-7210-2e9b-e053-2a95a90adfaf
NDC15631-0433
Product TypeHuman Otc Drug
Proprietary NameTELLURIUM METALLICUM
Generic NameTellurium Metallicum
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 NameTELLURIUM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0433-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0433-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0433-4 [15631043304]

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

NDC 15631-0433-0 [15631043300]

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

NDC 15631-0433-3 [15631043303]

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

NDC 15631-0433-5 [15631043305]

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

NDC 15631-0433-1 [15631043301]

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

NDC 15631-0433-2 [15631043302]

TELLURIUM METALLICUM 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
TELLURIUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:b141acaa-2683-4848-a6ac-cef9c6d0b213
Manufacturer
UNII

NDC Crossover Matching brand name "TELLURIUM METALLICUM" or generic name "Tellurium Metallicum"

NDCBrand NameGeneric Name
0220-4939Tellurium metallicumTELLURIUM
0220-4953Tellurium metallicumTELLURIUM
15631-0433TELLURIUM METALLICUMTELLURIUM METALLICUM
15631-0696TELLURIUM METALLICUMTELLURIUM METALLICUM
37662-1285Tellurium MetallicumTellurium Metallicum
37662-1286Tellurium MetallicumTellurium Metallicum
37662-1287Tellurium MetallicumTellurium Metallicum
37662-1288Tellurium MetallicumTellurium Metallicum
37662-1289Tellurium MetallicumTellurium Metallicum
37662-1290Tellurium MetallicumTellurium Metallicum
37662-1291Tellurium MetallicumTellurium Metallicum
37662-1292Tellurium MetallicumTellurium Metallicum
68428-667Tellurium metallicumTELLURIUM
71919-668TELLURIUM METALLICUMTellurium

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