FDA.reportPublic FDA data

Tiamulin Fumarate

Manufacturer
Jiangsu SEL Biochem Co., LTD. | SEL Biochem Xinjiang Co., Ltd.
Effective date
2021-07-21
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
3
Source
full-release
Hydrated at
2026-06-01 02:50:04

Label at a glance#

ProductTiamulin Fumarate
Active ingredientTIAMULIN FUMARATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 58735-0197-1
TIAMULIN FUMARATE
Content: 97.0 ~102.0% CAS No.: 55279-96-6
Manufacturing Date: Batch No.:
Retest Period: Three Years Net Weight: 25kg /drum
Caution: For Further Manufacturing, Processing or Repackaging. Federal Law Prohibits Dispensing Without Prescription.
Storage Conditions: Preserve in tight, light-resistant containers, and store at 30oC, excursions permitted to 40oC.
MANUFACTURER:
SEL BIOCHEM XINJIANG CO., LTD.
No. 3 Tianshan Road, Shihezi, Xinjiang, China
TEL: +86 571 88219588 FAX: +86 571 88210515

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58735-0197-1Tiamulin Fumarate25 kg in 1 PACKAGEPOWDER253
58735-0197-1Tiamulin Fumarate1 in 1 DRUMPOWDER13
58735-0197-2Tiamulin Fumarate1 in 1 DRUMPOWDER13
58735-0197-2Tiamulin Fumarate50 kg in 1 PACKAGEPOWDER503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58735-0197TIAMULIN FUMARATE POWDER [JIANGSU SEL BIOCHEM CO., LTD.]34 package rows20210722_e09e3524-9ef7-471d-b225-193dd931a3f1.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
58735-019758735-0197-1, 58735-0197-2

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
TIAMULIN FUMARATEION1Q02ZCXACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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