NDC 15631-0037

ANTIMONIUM IODATUM

Antimonium Iodatum

ANTIMONIUM IODATUM 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 Antimony Triiodide.

Product ID15631-0037_0b70eac8-1eda-43b3-8dcf-5ef45e1b09ef
NDC15631-0037
Product TypeHuman Otc Drug
Proprietary NameANTIMONIUM IODATUM
Generic NameAntimonium Iodatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameANTIMONY TRIIODIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0037-0

100 PELLET in 1 PACKAGE (15631-0037-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0037-0 [15631003700]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0037-4 [15631003704]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0037-1 [15631003701]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0037-2 [15631003702]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0037-5 [15631003705]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

NDC 15631-0037-3 [15631003703]

ANTIMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-18

Drug Details

Active Ingredients

IngredientStrength
ANTIMONY TRIIODIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:82dac837-0be2-44a3-b3f5-92896e8fb94d
Manufacturer
UNII

NDC Crossover Matching brand name "ANTIMONIUM IODATUM" or generic name "Antimonium Iodatum"

NDCBrand NameGeneric Name
0220-0377Antimonium iodatumANTIMONY TRIIODIDE
15631-0037ANTIMONIUM IODATUMANTIMONIUM IODATUM
63545-019Antimonium IodatumAntimonium Iodatum
63545-020Antimonium IodatumAntimonium Iodatum
63545-021Antimonium IodatumAntimonium Iodatum
63545-022Antimonium IodatumAntimonium Iodatum
63545-023Antimonium IodatumAntimonium Iodatum
63545-024Antimonium IodatumAntimonium Iodatum
63545-025Antimonium IodatumAntimonium Iodatum
68428-884Antimonium iodatumANTIMONY TRIIODIDE
71919-062Antimonium iodatumANTIMONY TRIIODIDE

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