Ruthenium bromatum
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2017-11-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:08:58
Label at a glance#
ProductRuthenium bromatum
Active ingredientRUTHENIUM TRIBROMIDE
Label structure1 sections
Label contents#
Full prescribing information#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | 00000 | Ruth brom.jpg, 5e83b790-e29c-4a82-e053-2991aa0a7a69.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-693-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-f31f-f424-e053-dadaa90a57ce | 5e808c4a-b3c5-0a05-e053-2991aa0a42a2 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-693-01 | Ruthenium bromatum | 240 [hp_C] in 1 VIAL, GLASS | PELLET | 240 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Ruthenium bromatum
- RUTHENIUM TRIBROMIDE
- RUTHENIUM
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-693 | 63545-693-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| RUTHENIUM TRIBROMIDE | VJ7MYGN19I | ACTIB |
| SUCROSE | C151H8M554 | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5e808c4a-b3c6-0a05-e053-2991aa0a42a2 | 5e808c4a-b3c5-0a05-e053-2991aa0a42a2 | 2017-11-21 | 5e808c4a-b3c6-0a05-e053-2991aa0a42a2 5e808c4a-b3c5-0a05-e053-2991aa0a42a2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
