FDA.reportPublic FDA data

NDC 85160-300-01 - Turkfleks 5% Dextrose Water Solution

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
85160-300
Requested NDC
85160-300-01
Package NDCs from labels
85160-300-01, 85160-300-10, 85160-300-02, 85160-300-20, 85160-300-03, 85160-300-30, 85160-300-04, 85160-300-40, 85160-300-05, 85160-300-50
Manufacturer
TURK ILAC VE SERUM SANAYI
Effective date
2025-03-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Turkfleks 5% Dextrose Water Solution - TURK ILAC VE SERUM SANAYITURK ILAC VE SERUM SANAYI2025-03-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85160-300-01Turkfleks 5% Dextrose Water Solution100 mL in 1 BAGINJECTION1001
85160-300-02Turkfleks 5% Dextrose Water Solution150 mL in 1 BAGINJECTION1501
85160-300-03Turkfleks 5% Dextrose Water Solution250 mL in 1 BAGINJECTION2501
85160-300-04Turkfleks 5% Dextrose Water Solution500 mL in 1 BAGINJECTION5001
85160-300-05Turkfleks 5% Dextrose Water Solution1000 mL in 1 BAGINJECTION10001
85160-300-10Turkfleks 5% Dextrose Water Solution100 in 1 BOXINJECTION1001
85160-300-20Turkfleks 5% Dextrose Water Solution100 in 1 BOXINJECTION1001
85160-300-30Turkfleks 5% Dextrose Water Solution100 in 1 BOXINJECTION1001
85160-300-40Turkfleks 5% Dextrose Water Solution100 in 1 BOXINJECTION1001
85160-300-50Turkfleks 5% Dextrose Water Solution50 in 1 BOXINJECTION501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85160-300TURKFLEKS 5% DEXTROSE WATER SOLUTION (5% DEXTROSE WATER SOLUTION) INJECTION [TURK ILAC VE SERUM SANAYI]110 package rows20250403_31ab2a1b-250d-5fc8-e063-6294a90a7359.zip

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.

Matched openFDA labels page 2 of 2 · 21 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DextroseDEXTROSE MONOHYDRATEBaxter Healthcare Company7de48bdb-9a05-4f2a-bbff-dcfeb284ca6e2020-02-27Warnings, Adverse reactionsExact identifier
rxcui: 1795609

Reported adverse events (FAERS/openFDA)#

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