FDA.reportPublic FDA data

Ticarcillin Sodium/Potassium Clavulanate

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-04-15
Label type
BULK INGREDIENT
Version
4
Source
full-release
Hydrated at
2026-06-01 02:49:58

Label at a glance#

ProductTicarcillin Sodium/Potassium Clavulanate
Active ingredientTICARCILLIN DISODIUM, CLAVULANATE POTASSIUM
Label structure1 sections

Label contents#

Full prescribing information#

Ticarcillin Sodium / Potassium Clavulanate (30:1)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
502415e5-4ac7-4266-a01a-ef44aa3c028dProduct name720250623
d0f377c9-74d8-e2e3-e06e-4d37534f5c0fProduct name320250620
ebb3e917-326a-9e18-0354-a19c9f63a2f3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-200-01Ticarcillin Sodium/Potassium Clavulanate1 kg in 1 CANISTERPOWDER14
73309-200-02Ticarcillin Sodium/Potassium Clavulanate0.9 kg in 1 JARPOWDER0.94
73309-200-03Ticarcillin Sodium/Potassium Clavulanate1.9 kg in 1 CANISTERPOWDER1.94
73309-200-04Ticarcillin Sodium/Potassium Clavulanate5 kg in 1 DRUMPOWDER54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-200TICARCILLIN SODIUM/POTASSIUM CLAVULANATE POWDER [BLUEBAY SHANDONG CO.,LTD]44 package rows20210417_4fa1526b-a8c9-4e7f-bdc0-c0138ce2466e.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-20073309-200-01, 73309-200-02, 73309-200-03, 73309-200-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
TICARCILLIN DISODIUMG8TVV6DSYGACTIM
CLAVULANATE POTASSIUMQ42OMW3AT8ACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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