FDA.reportPublic FDA data

NDC 85160-200-01 - Turkfleks %0.9 Sodium Chloride

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
85160-200
Requested NDC
85160-200-01
Package NDCs from labels
85160-200-01, 85160-200-10, 85160-200-02, 85160-200-20, 85160-200-03, 85160-200-30, 85160-200-04, 85160-200-40, 85160-200-05, 85160-200-50, 85160-200-06, 85160-200-60, 85160-200-07, 85160-200-70
Manufacturer
TURK ILAC VE SERUM SANAYI ANONIM SIRKETI
Effective date
2025-03-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Turkfleks %0.9 Sodium Chloride - TURK ILAC VE SERUM SANAYI ANONIM SIRKETITURK ILAC VE SERUM SANAYI ANONIM SIRKETI2025-03-28HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85160-200-01Turkfleks %0.9 Sodium Chloride50 mL in 1 BAGINJECTION, SOLUTION501
85160-200-02Turkfleks %0.9 Sodium Chloride100 mL in 1 BAGINJECTION, SOLUTION1001
85160-200-03Turkfleks %0.9 Sodium Chloride150 mL in 1 BAGINJECTION, SOLUTION1501
85160-200-04Turkfleks %0.9 Sodium Chloride250 mL in 1 BAGINJECTION, SOLUTION2501
85160-200-05Turkfleks %0.9 Sodium Chloride500 mL in 1 BAGINJECTION, SOLUTION5001
85160-200-06Turkfleks %0.9 Sodium Chloride1000 mL in 1 BAGINJECTION, SOLUTION10001
85160-200-07Turkfleks %0.9 Sodium Chloride3000 mL in 1 BAGINJECTION, SOLUTION30001
85160-200-10Turkfleks %0.9 Sodium Chloride100 in 1 BOXINJECTION, SOLUTION1001
85160-200-20Turkfleks %0.9 Sodium Chloride50 in 1 BOXINJECTION, SOLUTION501
85160-200-30Turkfleks %0.9 Sodium Chloride50 in 1 BOXINJECTION, SOLUTION501
85160-200-40Turkfleks %0.9 Sodium Chloride25 in 1 BOXINJECTION, SOLUTION251
85160-200-50Turkfleks %0.9 Sodium Chloride20 in 1 BOXINJECTION, SOLUTION201
85160-200-60Turkfleks %0.9 Sodium Chloride20 in 1 BOXINJECTION, SOLUTION201
85160-200-70Turkfleks %0.9 Sodium Chloride10 in 1 BOXINJECTION, SOLUTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
85160-200TURKFLEKS %0.9 SODIUM CHLORIDE (%0.9 SODIUM CHLORIDE) INJECTION, SOLUTION [TURK ILAC VE SERUM SANAYI ANONIM SIRKETI]114 package rows20250402_3170d1ee-c6c9-5c35-e063-6294a90a5f04.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 3 of 3 · 48 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0.9% SODIUM CHLORIDESODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirstc755e41b-acba-7234-e053-2995a90aff0f2021-07-17Warnings, Adverse reactionsExact identifier
rxcui: 1807634
SODIUM CHLORIDESODIUM CHLORIDEBaxter Healthcare Corporationaeaed9cb-b629-4019-88d2-a916179427de2021-02-19Warnings, Adverse reactionsExact identifier
rxcui: 1807631
rxcui: 1807632
Met-ToxARSENICUM ALBUM, AVENA SATIVA,LYCOPODIUM CLAVATUM,NATRUM MURIATICUM,NUX VOMICA,PHYTOLACCA DECANDRARHAMNUS FRANGULA,SOLIDAGO VIRGAUREA,TRIFOLIUM PRATENSE,HEAVY METAL NOSODESwHITE mANUFACTURING INC DBA MICRO-WESTe65db4c2-0bc7-4c50-8f18-b36ee004c4f52021-01-21WarningsExact identifier
unii: Q32ZN48698
SODIUM CHLORIDESODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirstac0fd44a-3f39-8d7e-e053-2995a90afeec2020-08-04Warnings, Adverse reactionsExact identifier
rxcui: 1807634
0.9% SODIUM CHLORIDE0.9% SODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirsta62b71db-8ba2-6f6b-e053-2a95a90a29d12020-05-21Warnings, Adverse reactionsExact identifier
rxcui: 1807632
0.9% SODIUM CHLORIDE0.9% SODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirsta2b8220f-e33a-51c3-e053-2995a90a07342020-04-07Warnings, Adverse reactionsExact identifier
rxcui: 1807633
0.9% SODIUM CHLORIDE0.9% SODIUM CHLORIDEHF Acquisition Co LLC, DBA HealthFirsta2bba76a-08ce-6902-e053-2995a90ab9c92020-04-07Warnings, Adverse reactionsExact identifier
rxcui: 1807639
Sodium ChlorideSODIUM CHLORIDEBaxter Healthcare Corporationfbc01464-8885-4075-af41-911ffec5ae922020-01-27Warnings, Adverse reactionsExact identifier
rxcui: 1807631
rxcui: 1807632

Reported adverse events (FAERS/openFDA)#

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