Paromomycin Sulfate
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2019-08-21
- Label type
- BULK INGREDIENT
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:49:20
Label at a glance#
ProductParomomycin Sulfate
Active ingredientPAROMOMYCIN SULFATE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-018-01 | Paromomycin Sulfate | 1 kg in 1 JAR | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Paromomycin Sulfate
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73309-018 | 73309-018-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PAROMOMYCIN SULFATE | 845NU6GJPS | ACTIM |
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 |
|---|---|---|---|---|---|---|
| Humatin | PAROMOMYCIN SULFATE | Waylis Therapeutics LLC | a725f022-ec3c-430d-8021-96c861b9893c | 2025-11-13 | Adverse reactions | PAROMOMYCIN SULFATE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
