NDC 15631-0028

AMMONIUM IODATUM

Ammonium Iodatum

AMMONIUM 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 Ammonium Iodide.

Product ID15631-0028_6eee3c37-2b00-4e3a-b510-c39485d3aa36
NDC15631-0028
Product TypeHuman Otc Drug
Proprietary NameAMMONIUM IODATUM
Generic NameAmmonium Iodatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAMMONIUM IODIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0028-5

12500 PELLET in 1 PACKAGE (15631-0028-5)
Marketing Start Date2015-10-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0028-3 [15631002803]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

NDC 15631-0028-5 [15631002805]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

NDC 15631-0028-4 [15631002804]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

NDC 15631-0028-2 [15631002802]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

NDC 15631-0028-0 [15631002800]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

NDC 15631-0028-1 [15631002801]

AMMONIUM IODATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-10-02
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM IODIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:4a77a97a-14fe-458d-9911-24306b9c431a
Manufacturer
UNII

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