NDC 49230-300
Sodium Chloride 900 mg per 100 mL injection
On the label: Fresenius Medical Care Renal Therapies Group, LLC.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Fresenius Medical Care Renal Therapies Group, LLC names for other drugs.
Recalls
- May 27, 2025 · Class II · Fresenius Medical Care Holdings, Inc.
Lack of Assurance of Sterility
Lots: 24PU06037, 24PU06038, 24PU06040, 24PU06041, 24PU06042, 24PU06043, 24PU06044, 24PU06045, 24PU0646, 24PU06047, 24PU06048, 24PU06049, 24PU06050, 24PU06052, 24PU06053, 24PU06054 & 24PU06055, Exp Date 11/30/2025; 24SU06001, 24SU06002, 24SU06003, 24SU06004, 24SU06005, 24SU06006, 24SU06007, 24SU06009, 24… - May 23, 2023 · Class II · Fresenius Medical Care Holdings, Inc.
Lack of assurance of sterility: The product was potentially exposed to below-recommended storage temperatures, which may cause leaks in the packaging.
Lots: Lot # 23AU05030, Exp 01/13/2024; 23AU05035, Exp 01/15/2024 - Nov 22, 2022 · Class II · Fresenius Medical Care Holdings, Inc.
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Lots: Lot # 22HU05062, 22HU06059, 22HU05035, EXP 06/30/2023; 22JU05001, EXP 07/31/2023 - Oct 11, 2022 · Class II · Fresenius Medical Care Holdings, Inc.
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Lots: Lot # 22EU05043, EXP 5/21/2023; 22HU05018, EXP 6/9/2023; 22HU05019, EXP 6/10/2023; 22HU05025, 22HU05026, EXP 6/12/2023; 22HU05049, EXP 6/22/2023; 22HU05053, EXP 6/24/2023; 22HU05054, 22HU05055, EXP 6/25/2023; 22HU06027, EXP 6/11/2023; 22HU06049, EXP 6/23/2023; 22HU06055, EXP 6/24/2023; 22HU06056, E…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, intravenous
- Strength
- 900 mg per 100 mL
- Approval
- ANDA ANDA078177
- On the market since
- Apr 12, 2007
- Package NDCs
49230-300-10- Official label
- DailyMed (National Library of Medicine), updated Jul 27, 2026
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