Tylosin Phosphate

Manufacturer
Biovet Joint Stock Company
Effective date
2022-01-12
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
full-release
Hydrated at
2026-06-01 02:50:20

Label at a glance#

ProductTylosin Phosphate
Active ingredientTYLOSIN PHOSPHATE
Label structure2 sections

Label contents#

Full prescribing information#

DRUM LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TYLOSIN PHOSPHATE

ACTIVE PHARMACEUTICAL INGREDIENT

BATCH No:

NET WEIGHT: 

GROSS WEIGHT:
MANUFACTURE DATE:
EXPIRATION DATE:

STORE AT OR BELOW 25°C, EXCURSIONS PERMITTED BEWTWEEN 15°C and 30°C.
PRESERVE IN WELL-CLOSED CONTAINER, PROTECTED FROM LIGHT, MOISTURE,

AND EXCESSIVE HEAT.

FOR MANUFACTURING, PROCESSING OR REPACKING.

FOR ANIMAL USE ONLY!

PRODUCT MANUFACTURED IN BULGARIA

MANUFACTURED BY:
BIOVET JSC., 39 Petar Rakov St.,

Peshtera 4550, Bulgaria

Drum Label Image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drum Label ImageDrum Label Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11311-799-252019-10-21C16284748780-1956f9ecf-cb22-621f-e053-dbdaa90a74adTYLOSIN PHOSPHATE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11311-799-25Tylosin Phosphate25 kg in 1 DRUMPOWDER252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11311-799TYLOSIN PHOSPHATE POWDER [BIOVET JOINT STOCK COMPANY]21 package rows20220119_59e7addc-2891-44da-ac7d-27f36447c463.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11311-79911311-799-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
TYLOSIN PHOSPHATENR75X12AFFACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.