Sodium Chloride
Average across 2 priced NDCs. A benchmark of pharmacy acquisition cost - not a retail quote.
Prescriptions dispensed under Medicaid (fee-for-service + managed care), summed nationally. The closest free proxy to sales volume - Medicaid only, not all-payer.
US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.
| Labeler | Type | Packages | Status |
|---|---|---|---|
| Baxter Healthcare Corporation | brand | 14 | SUPPLYING |
| Nephron Pharmaceuticals Corporation | unknown | 4 | SUPPLYING |
| Fresenius Kabi, USA LLC | generic | 3 | SUPPLYING |
| Henry Schein, Inc. | relabeler | 1 | SUPPLYING |
| Fresenius Medical Care Renal Therapies Group, LLC | unknown | 1 | SUPPLYING |
| Fresenius Medical Care de Mexico, S.A. de C.V. | unknown | 1 | SUPPLYING |
| Cardinal Health 107, LLC | repackager | 1 | SUPPLYING |
| B. Braun Medical Inc. | unknown | 1 | SUPPLYING |
Shortages, recalls, and registration changes attached to this drug concept.
Lack of Assurance of Sterility — Recalling firm: Fresenius Medical Care Holdings, Inc. — Nationwide.
Lack of assurance of sterility: The product was potentially exposed to below-recommended storage temperatures, which may cause leaks in the packaging. — Recalling firm: Fresenius Medical Care Holdings, Inc. — Product was distributed to 32 clinics in SC, NC and VA.
CGMP Deviations: potential for trace amounts of product carryover. — Recalling firm: Nephron Sc Inc — Nationwide in the USA
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution. — Recalling firm: Fresenius Medical Care Holdings, Inc. — Product was distributed Nationwide in the USA.
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution. — Recalling firm: Fresenius Medical Care Holdings, Inc. — Nationwide in the USA
Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the stoppers do not contain natural rubber latex. The tray label for these two product codes and the vial label for product code 918620 also incorrectly state that the stoppers do not contain latex. The above listed product codes and batches being recalled have stoppers containing natural rubber latex. — Recalling firm: Fresenius Kabi USA, LLC — Distributed Nationwide in the USA and Puerto RIco
Labeling Not Elsewhere Classified: Fresenius Kabi is taking this action due to an incorrect statement on the product insert for product codes 918610 and 918620 indicating that the stoppers do not contain natural rubber latex. The tray label for these two product codes and the vial label for product code 918620 also incorrectly state that the stoppers do not contain latex. The above listed product codes and batches being recalled have stoppers containing natural rubber latex. — Recalling firm: Fresenius Kabi USA, LLC — Distributed Nationwide in the USA and Puerto RIco
Lack of Assurance of Sterility: potential for leaking containers which lacks the assurance of sterility. — Recalling firm: Baxter Healthcare Corp. — Nationwide and Puerto Rico
Presence of Particulate Matter: identified as cardboard. — Recalling firm: Baxter Healthcare Corp. — Nationwide and Puerto Rico
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled. — Recalling firm: Baxter Healthcare Corp. — Nationwide
Presence of Particulate Matter: Confirmed customer complaints received for the presence of blue plastic, identified as fragments of the frangible from the vial adapter. — Recalling firm: Baxter Healthcare Corp — Nationwide and Puerto Rico.
Presence of Particulate Matter: particulate matter identified as fibers and/or plastics. — Recalling firm: Baxter Healthcare Corp. — Nationwide, Puerto Rico, Singapore, and Hong Kong
Lack of Assurance of Sterility: Specific lot numbers of these products have been identified for potential administration port leakage. The potential for leakage is the result of a manufacturing issue which occurred during the sealing of the closure assembly at the administration port. — Recalling firm: Baxter Healthcare Corp. — Nationwide & Puerto Rico
Labeling Wrong Barcode; It may display wrong product code reflecting 0.9% Sodium Chloride Injection , USP 100 mL in MINI-BAG Plus container instead of 50 mL. — Recalling firm: Baxter Healthcare Corp. — Nationwide and Singapore
