NDC 85160-400-01 - TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE 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
- 85160-400
- Requested NDC
- 85160-400-01
- Package NDCs from labels
- 85160-400-01, 85160-400-10, 85160-400-02, 85160-400-20, 85160-400-03, 85160-400-30, 85160-400-04, 85160-400-40, 85160-400-05, 85160-400-50, 85160-400-06, 85160-400-60, 85160-400-07, 85160-400-70
- Manufacturer
- TURK ILAC VE SERUM SANAYI
- Effective date
- 2025-04-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution - TURK ILAC VE SERUM SANAYI | TURK ILAC VE SERUM SANAYI | 2025-04-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85160-400-01 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 50 mL in 1 BAG | INJECTION, SOLUTION | 50 | 1 | |
| 85160-400-02 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 100 mL in 1 BAG | INJECTION, SOLUTION | 100 | 1 | |
| 85160-400-03 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 150 mL in 1 BAG | INJECTION, SOLUTION | 150 | 1 | |
| 85160-400-04 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | 1 | |
| 85160-400-05 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | 1 | |
| 85160-400-06 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | 1 | |
| 85160-400-07 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 3000 mL in 1 BAG | INJECTION, SOLUTION | 3000 | 1 | |
| 85160-400-10 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 100 in 1 BOX | INJECTION, SOLUTION | 100 | 1 | |
| 85160-400-20 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 50 in 1 BOX | INJECTION, SOLUTION | 50 | 1 | |
| 85160-400-30 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 50 in 1 BOX | INJECTION, SOLUTION | 50 | 1 | |
| 85160-400-40 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 25 in 1 BOX | INJECTION, SOLUTION | 25 | 1 | |
| 85160-400-50 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 20 in 1 BOX | INJECTION, SOLUTION | 20 | 1 | |
| 85160-400-60 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 20 in 1 BOX | INJECTION, SOLUTION | 20 | 1 | |
| 85160-400-70 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE Solution | 10 in 1 BOX | INJECTION, SOLUTION | 10 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 85160-400 | TURKFLEKS 0.9% ISOTONIC SODIUM CHLORIDE SOLUTION (0.9% ISOTONIC SODIUM CHLORIDE SOLUTION) INJECTION, SOLUTION [TURK ILAC VE SERUM SANAYI] | 1 | 14 package rows | 20250406_31d4876a-87c3-c0ab-e063-6294a90ada57.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sodium Chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | 4829ee40-c2d7-4e17-a606-75e8a8628413 | 2021-12-21 | Warnings, Adverse reactions | 1807634 |
| 0.9% SODIUM CHLORIDE | SODIUM CHLORIDE | HF Acquisition Co LLC, DBA HealthFirst | c755e41b-acba-7234-e053-2995a90aff0f | 2021-07-17 | Warnings, Adverse reactions | 1807634 |
| Met-Tox | ARSENICUM ALBUM, AVENA SATIVA,LYCOPODIUM CLAVATUM,NATRUM MURIATICUM,NUX VOMICA,PHYTOLACCA DECANDRARHAMNUS FRANGULA,SOLIDAGO VIRGAUREA,TRIFOLIUM PRATENSE,HEAVY METAL NOSODES | wHITE mANUFACTURING INC DBA MICRO-WEST | e65db4c2-0bc7-4c50-8f18-b36ee004c4f5 | 2021-01-21 | Warnings | Q32ZN48698 |
| SODIUM CHLORIDE | SODIUM CHLORIDE | HF Acquisition Co LLC, DBA HealthFirst | ac0fd44a-3f39-8d7e-e053-2995a90afeec | 2020-08-04 | Warnings, Adverse reactions | 1807634 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.