NDC 15631-0542
BROMIUM
Bromium
BROMIUM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Bromine.
| Product ID | 15631-0542_caac2afe-9588-44be-b8e9-42aa392f801c |
| NDC | 15631-0542 |
| Product Type | Human Otc Drug |
| Proprietary Name | BROMIUM |
| Generic Name | Bromium |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-12-30 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc |
| Substance Name | BROMINE |
| Active Ingredient Strength | 6 [hp_X]/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 15631-0542-1
4 TABLET in 1 BLISTER PACK (15631-0542-1)
| Marketing Start Date | 2015-12-30 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 15631-0542-3 [15631054203]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-6 [15631054206]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-2 [15631054202]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-0 [15631054200]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-1 [15631054201]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-4 [15631054204]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-7 [15631054207]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
NDC 15631-0542-5 [15631054205]
BROMIUM TABLET
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2015-12-30 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| BROMINE | 6 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | 4f0cf770-40ca-4c7b-a337-e48372d4e5f5 |
| Manufacturer | |
| UNII | |
| UPC Code |
NDC Crossover Matching brand name "BROMIUM" or generic name "Bromium"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0220-0901 | Bromium | BROMINE |
| 0220-0904 | Bromium | BROMINE |
| 0220-0907 | Bromium | Bromine |
| 0220-0909 | Bromium | BROMINE |
| 15631-0086 | BROMIUM | BROMIUM |
| 15631-0542 | BROMIUM | BROMIUM |
| 62106-4927 | BROMIUM | Bromine |
| 63545-540 | Bromium | Bromium |
| 63545-541 | Bromium | Bromium |
| 63545-542 | Bromium | Bromium |
| 63545-543 | Bromium | Bromium |
| 63545-544 | Bromium | Bromium |
| 63545-545 | Bromium | Bromium |
| 63545-546 | Bromium | Bromium |
| 63545-547 | Bromium | Bromium |
| 68428-264 | Bromium | BROMINE |
| 71919-131 | Bromium | BROMINE |
| 69152-1039 | Bromium 30C | Bromium |
| 69152-1176 | Bromium 6C | Bromium |
Trademark Results [BROMIUM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BROMIUM 85545739 4777466 Live/Registered |
Bromium Inc. 2012-02-17 |
 BROMIUM 85444376 4306128 Live/Registered |
Bromium Inc. 2011-10-11 |
 BROMIUM 85361323 not registered Dead/Abandoned |
BROMIUM, INC. 2011-07-01 |
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