Tylosin Tartrate
- Manufacturer
- DARMERICA, LLC
- Effective date
- 2026-01-09
- Label type
- BULK INGREDIENT - ANIMAL DRUG
- Version
- 4
- Source
- monthly-update
- Hydrated at
- 2026-06-03 17:53:27
Label at a glance#
ProductTylosin Tartrate
Active ingredientTylosin Tartrate
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71052-190-00 | Tylosin Tartrate | 0.5 kg in 1 PACKAGE | POWDER | 0.5 | 4 | |
| 71052-190-05 | Tylosin Tartrate | 5 kg in 1 PACKAGE | POWDER | 5 | 4 | |
| 71052-190-10 | Tylosin Tartrate | 0.10 kg in 1 PACKAGE | POWDER | 0.10 | 4 | |
| 71052-190-20 | Tylosin Tartrate | 1 kg in 1 PACKAGE | POWDER | 1 | 4 |
Products#
Every source-derived product name is available through these pages.
- Tylosin Tartrate
- TYLOSIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 71052-190 | 71052-190-20, 71052-190-05, 71052-190-00, 71052-190-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Tylosin Tartrate | 5P4625C51T | ACTIB |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 3 | 2024-12-26 | full-release | 2026-06-01 02:51:22 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
