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 | Type |
|---|---|---|---|
| Turkfleks %0.9 Sodium Chloride - TURK ILAC VE SERUM SANAYI ANONIM SIRKETI | TURK ILAC VE SERUM SANAYI ANONIM SIRKETI | 2025-03-28 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85160-200-01 | Turkfleks %0.9 Sodium Chloride | 50 mL in 1 BAG | INJECTION, SOLUTION | 50 | 1 | |
| 85160-200-02 | Turkfleks %0.9 Sodium Chloride | 100 mL in 1 BAG | INJECTION, SOLUTION | 100 | 1 | |
| 85160-200-03 | Turkfleks %0.9 Sodium Chloride | 150 mL in 1 BAG | INJECTION, SOLUTION | 150 | 1 | |
| 85160-200-04 | Turkfleks %0.9 Sodium Chloride | 250 mL in 1 BAG | INJECTION, SOLUTION | 250 | 1 | |
| 85160-200-05 | Turkfleks %0.9 Sodium Chloride | 500 mL in 1 BAG | INJECTION, SOLUTION | 500 | 1 | |
| 85160-200-06 | Turkfleks %0.9 Sodium Chloride | 1000 mL in 1 BAG | INJECTION, SOLUTION | 1000 | 1 | |
| 85160-200-07 | Turkfleks %0.9 Sodium Chloride | 3000 mL in 1 BAG | INJECTION, SOLUTION | 3000 | 1 | |
| 85160-200-10 | Turkfleks %0.9 Sodium Chloride | 100 in 1 BOX | INJECTION, SOLUTION | 100 | 1 | |
| 85160-200-20 | Turkfleks %0.9 Sodium Chloride | 50 in 1 BOX | INJECTION, SOLUTION | 50 | 1 | |
| 85160-200-30 | Turkfleks %0.9 Sodium Chloride | 50 in 1 BOX | INJECTION, SOLUTION | 50 | 1 | |
| 85160-200-40 | Turkfleks %0.9 Sodium Chloride | 25 in 1 BOX | INJECTION, SOLUTION | 25 | 1 | |
| 85160-200-50 | Turkfleks %0.9 Sodium Chloride | 20 in 1 BOX | INJECTION, SOLUTION | 20 | 1 | |
| 85160-200-60 | Turkfleks %0.9 Sodium Chloride | 20 in 1 BOX | INJECTION, SOLUTION | 20 | 1 | |
| 85160-200-70 | Turkfleks %0.9 Sodium Chloride | 10 in 1 BOX | INJECTION, SOLUTION | 10 | 1 |
DailyMed Dashboard NDC Coverage#
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 | Baxter Healthcare Corporation | 93aeac13-41de-4452-9f38-d6b4f38ada30 | 2025-01-24 | 1807639 1807634 1807633 | |
| 0.9% SODIUM CHLORIDE | 0.9% SODIUM CHLORIDE | HF Acquisition Co LLC, DBA HealthFirst | 8dfb05c0-77e8-2fa1-e053-2a95a90a3d33 | 2025-01-08 | Adverse reactions | 1807631 |
| Dyural 80 Kit | METHYLPREDNISOLONE ACETATE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE, SODIUM CHLORIDE, ISOPROPYL ALCOHOL | Advanced Rx Pharmacy of Tennessee, LLC | 01ca2f07-9c84-e418-e063-6294a90ac760 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 1807631 |
| Dyural 40 Kit | METHYLPREDNISOLONE ACETATE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE, SODIUM CHLORIDE, ISOPROPYL ALCOHOL | Advanced Rx Pharmacy of Tennessee, LLC | 01ca16de-ab2e-4e19-e063-6394a90a0510 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 1807631 |
| Sodium Chloride | SODIUM CHLORIDE | Hospira, Inc. | 8eb172da-dcd4-4660-4a8f-ad44a14b4af7 | 2024-11-06 | Adverse reactions | 1807631 |
| Trace Mineral Cord | ALUMINUM, ANTIMONY, BARIUM, BERYLLIUM, BISMUTH, BORON, BROMINE, CALCIUM, CARBON, CERIUM, CESIUM, CHLORIDE, CHROMIUM, COBALT, COPPER, DYSPROSIUM, ERBIUM, EUROPIUM, FLUORIDE, GADOLINIUM, GALLIUM, GERMANIUM, GOLD, HAFNIUM, HOLMIUM, INDIUM, IODINE, IRIDIUM, IRON, LANTHANUM, LITHIUM, LUTETIUM, MAGNESIUM, MANGANESE, MOLYBDENUM, NEODYMIUM, NICKEL, NIOBIUM, OSMIUM, PALLADIUM, PHOSPHORUS, PLATINUM, POTASSIUM, PRASEODYMIUM, RHENIUM, RHODIUM, RUBIDIUM, RUTHENIUM, SAMARIUM, SCANDIUM, SELENIUM, SILICON, SILVER | Energique, Inc. | 7a34327c-39fe-403b-87a0-4f3bea36bb2a | 2024-09-27 | Warnings | Q32ZN48698 |
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | f55bd888-5e01-474d-871b-24654c070178 | 2024-07-24 | Warnings, Adverse reactions | 1807627 1807631 1807639 1807634 1807633 1807632 |
| Sodium Chloride | SODIUM CHLORIDE | CODAN US CORPORATION | aa06e286-75c6-4d7a-959f-6008d38aa6e5 | 2024-06-24 | Warnings, Adverse reactions | 1807631 1807639 1807634 1807633 1807632 |
| Sodium chloride | SODIUM CHLORIDE | Becton Dickinson and Company | ebc8b008-a8b3-4c41-89e4-b413f7aab89f | 2024-05-21 | Warnings, Adverse reactions | 1807631 1807639 1807634 1807633 1807632 |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | 47a0313f-36df-4fa6-a828-c9e1946ba9b0 | 2024-05-08 | Warnings, Adverse reactions | 1807639 |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | 7f22c06b-6b4d-4b49-a4b2-d2169f2bd653 | 2024-05-07 | Warnings, Adverse reactions | 1807639 1807634 1807633 |
| Sodium chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | c1e52670-c85e-4f19-a2e9-bf9abd7c3727 | 2024-04-23 | Warnings, Adverse reactions | 1807631 1807639 1807634 1807633 1807632 |
| 0.9% SODIUM CHLORIDE | 0.9% SODIUM CHLORIDE | HF Acquisition Co LLC, DBA HealthFirst | e5247ed5-6170-c13f-e053-2a95a90a4101 | 2024-01-27 | Warnings, Adverse reactions | 1807634 |
| Sodium chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | 037ac04d-f8f3-4bb8-993a-ac8f7683ff83 | 2024-01-04 | Warnings, Adverse reactions | 1807631 1807639 1807634 1807633 1807632 |
| Pituistat | ARALIA QUINQUEFOLIA, GINKGO BILOBA, ARSENICUM IODATUM, AVENA SATIVA, BARYTA CARBONICA, PHOSPHORUS, SILICEA, THYROIDINUM (SUIS), ALUMINUM, ANTIMONY, BARIUM, BERYLLIUM, BISMUTH, BORON, BROMINE, CALCIUM, CARBON, CERIUM, CESIUM, CHLORIDE, CHROMIUM, COBALT, COPPER, DYSPROSIUM, ERBIUM, EUROPIUM, FLUORIDE, GADOLINIUM, GALLIUM, GERMANIUM, GOLD, HAFNIUM, HOLMIUM, INDIUM, IODINE, IRIDIUM, IRON, LANTHANUM, LITHIUM, LUTETIUM, MAGNESIUM, MANGANESE, MOLYBDENUM, NEODYMIUM, NICKEL, NIOBIUM, OSMIUM, PALLADIUM | Energique, Inc. | 27a5fccb-8707-4bb5-a848-d1921bba2f7f | 2023-08-21 | Warnings | Q32ZN48698 |
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 2fae04e3-20b1-4b8c-b1fb-646b384836f1 | 2022-12-07 | Warnings, Adverse reactions | 1807631 1807632 |
| SODIUM CHLORIDE | SODIUM CHLORIDE | Baxter Healthcare Corporation | 123bd10a-90c7-499e-97f6-acf7e0f0fb4e | 2022-07-29 | Warnings, Adverse reactions | 1807631 1807632 |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | cc14fafd-3dcd-4fc8-bdbd-6f355c375768 | 2022-02-23 | Warnings, Adverse reactions | 1807631 1807632 |
| Sodium Chloride | SODIUM CHLORIDE | B. Braun Medical Inc. | e44c41ae-c9c8-4dd8-ba6c-cebb585378aa | 2022-01-31 | Warnings, Adverse reactions | 1807639 1807634 |
| Sodium Chloride | SODIUM CHLORIDE | Fresenius Kabi USA, LLC | 4829ee40-c2d7-4e17-a606-75e8a8628413 | 2021-12-21 | Warnings, Adverse reactions | 1807639 1807634 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.