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 ID | 15631-0028_6eee3c37-2b00-4e3a-b510-c39485d3aa36 |
NDC | 15631-0028 |
Product Type | Human Otc Drug |
Proprietary Name | AMMONIUM IODATUM |
Generic Name | Ammonium Iodatum |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2015-10-02 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
Substance Name | AMMONIUM IODIDE |
Active Ingredient Strength | 3 [hp_X]/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2015-10-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-10-02 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
AMMONIUM IODIDE | 3 [hp_X]/1 |
SPL SET ID: | 4a77a97a-14fe-458d-9911-24306b9c431a |
Manufacturer | |
UNII |