PillSodium Chloride
Sodium Chloride
8 active makers
soon
soon
soon
soon
US acquisition costNADAC · per unit
Average across 2 priced NDCs. A benchmark of pharmacy acquisition cost — not a retail quote.
Medicaid dispensing volumeSDUD · per quarter
Prescriptions dispensed under Medicaid (fee-for-service + managed care), summed nationally. The closest free proxy to sales volume — Medicaid only, not all-payer.
Who makes it8 active · 0 exited
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 | unknown | 14 | SUPPLYING |
| Nephron Pharmaceuticals Corporation | unknown | 4 | SUPPLYING |
| Fresenius Kabi USA, LLC | unknown | 3 | SUPPLYING |
| Henry Schein Inc. | unknown | 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 | unknown | 1 | SUPPLYING |
| B. Braun Medical Inc. | unknown | 1 | SUPPLYING |
Regulatory & supply eventsFDA · US
Shortages, recalls, and registration changes attached to this drug concept.
- May 27, 2025RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, Flexible Plastic Container, Rx Only Fresenius Medical Care North America, Waltham,…
Lack of Assurance of Sterility — Recalling firm: Fresenius Medical Care Holdings, Inc. — Nationwide.
- May 23, 2023RECALLRecall (Class II): Sodium Chloride 0.9% Injection, USP, 1000 mL bags, 12 bags per carton, Rx only, Fresenius Medical Care North America, W…
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.
- Jan 12, 2023RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, 100 mL Single-Dose Container bag, Rx Only, Nephron Pharmaceuticals Corporation, 45…
CGMP Deviations: potential for trace amounts of product carryover. — Recalling firm: Nephron Sc Inc — Nationwide in the USA
- Nov 22, 2022RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs…
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.
- Oct 11, 2022RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs…
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
- Nov 15, 2018RECALLRecall (Class I): SODIUM CHLORIDE INJECTION, USP, 0.9%, 20 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals,…
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
- Nov 15, 2018RECALLRecall (Class I): SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals,…
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
- Jan 21, 2016RECALLRecall (Class II): 0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter…
Lack of Assurance of Sterility: potential for leaking containers which lacks the assurance of sterility. — Recalling firm: Baxter Healthcare Corp. — Nationwide and Puerto Rico
- Jan 21, 2016RECALLRecall (Class I): 0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter…
Presence of Particulate Matter: identified as cardboard. — Recalling firm: Baxter Healthcare Corp. — Nationwide and Puerto Rico
- Jul 17, 2015RECALLRecall (Class I): 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter …
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
- Dec 4, 2014RECALLRecall (Class I): 0.9% Sodium Chloride Injection USP, 100 mL MINI-BAG Plus Container, Rx only, Baxter Healthcare Corporation, Deerfield, …
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.
- Jul 11, 2014RECALLRecall (Class I): 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter …
Presence of Particulate Matter: particulate matter identified as fibers and/or plastics. — Recalling firm: Baxter Healthcare Corp. — Nationwide, Puerto Rico, Singapore, and Hong Kong
- May 21, 2013RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, in MINI-BAG Plus Container, a) 50 mL (NDC 0338-0553-11), b) 100 mL (NDC 0338-0553-…
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
- Feb 27, 2013RECALLRecall (Class II): 0.9% Sodium Chloride Injection, USP, 50 mL Mini-Bag Plus Container, Rx only, distributed by Baxter Healthcare Corporati…
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