Ammonium Bromatum
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2020-09-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:13:20
Label at a glance#
ProductAmmonium Bromatum
Active ingredientAMMONIUM BROMIDE
Label structure1 sections
Label contents#
Full prescribing information#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-930-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7c56-a426-e053-dadaa90af4c2 | b0796c83-72bd-44e4-e053-2995a90a5fc7 |
| 63545-930-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7c56-a426-e053-dadaa90af4c2 | b0796c83-72bd-44e4-e053-2995a90a5fc7 |
| 63545-930-03 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7c56-a426-e053-dadaa90af4c2 | b0796c83-72bd-44e4-e053-2995a90a5fc7 |
| 63545-930-04 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7c56-a426-e053-dadaa90af4c2 | b0796c83-72bd-44e4-e053-2995a90a5fc7 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-930-01 | Ammonium Bromatum | 200 in 1 VIAL, GLASS | PELLET | 200 | 1 | |
| 63545-930-02 | Ammonium Bromatum | 500 in 1 VIAL, GLASS | PELLET | 500 | 1 | |
| 63545-930-03 | Ammonium Bromatum | 3000 in 1 BOTTLE, GLASS | PELLET | 3000 | 1 | |
| 63545-930-04 | Ammonium Bromatum | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Ammonium Bromatum
- SUCROSE
- AMMONIUM BROMIDE
- BROMIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-930 | 63545-930-01, 63545-930-02, 63545-930-03, 63545-930-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| AMMONIUM BROMIDE | R0JB3224WS | ACTIB |
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 |
|---|---|---|---|---|---|---|
| b0796c83-72be-44e4-e053-2995a90a5fc7 | b0796c83-72bd-44e4-e053-2995a90a5fc7 | 2020-09-29 | b0796c83-72be-44e4-e053-2995a90a5fc7 b0796c83-72bd-44e4-e053-2995a90a5fc7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.



