NDC 15631-0250

KALI IODATUM

Kali Iodatum

KALI 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 Potassium Iodide.

Product ID15631-0250_5be6ded4-f8cb-4895-8c95-46f8a21a28ab
NDC15631-0250
Product TypeHuman Otc Drug
Proprietary NameKALI IODATUM
Generic NameKali Iodatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePOTASSIUM IODIDE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0250-0

100 PELLET in 1 PACKAGE (15631-0250-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0250-4 [15631025004]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0250-5 [15631025005]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0250-2 [15631025002]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0250-1 [15631025001]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0250-3 [15631025003]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0250-0 [15631025000]

KALI IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM IODIDE1 [hp_X]/1

OpenFDA Data

SPL SET ID:58d88be2-bad9-4fcf-895e-03e48c8eb852
Manufacturer
UNII

NDC Crossover Matching brand name "KALI IODATUM" or generic name "Kali Iodatum"

NDCBrand NameGeneric Name
0220-2798Kali iodatumPOTASSIUM IODIDE
0220-2799Kali iodatumPOTASSIUM IODIDE
0220-2800Kali iodatumPOTASSIUM IODIDE
0220-2801Kali iodatumPOTASSIUM IODIDE
0220-2802Kali iodatumPOTASSIUM IODIDE
0220-2803Kali iodatumPOTASSIUM IODIDE
0220-2804Kali iodatumPOTASSIUM IODIDE
0220-2805Kali iodatumPOTASSIUM IODIDE
0220-2887Kali iodatumPOTASSIUM IODIDE
10191-1857KALI IODATUMPOTASSIUM IODIDE
15631-0250KALI IODATUMKALI IODATUM
15631-0610KALI IODATUMKALI IODATUM
37662-1489Kali IodatumKali Iodatum
37662-1490Kali IodatumKali Iodatum
37662-1491Kali IodatumKali Iodatum
37662-1492Kali IodatumKali Iodatum
37662-1493Kali IodatumKali Iodatum
37662-1494Kali IodatumKali Iodatum
37662-1495Kali IodatumKali Iodatum
37662-1496Kali IodatumKali Iodatum
68428-453Kali iodatumPOTASSIUM IODIDE
71919-383Kali iodatumPOTASSIUM IODIDE

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.