drug
SODIUM CHLORIDE
updated 6mo agoby LIEBEL-FLARSHEIM
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Trials studying SODIUM CHLORIDE
- phase2A Study to Evaluate the Efficacy, Safety, and Tolerability of CBL-514 Injection for Reducing Abdominal Subcutaneous Fat
- phase3A Study to Evaluate the Maintenance of Efficacy and Long-term Safety of CBL-514 Injection for Reducing Subcutaneous Fat (Stage 1)
- phase2Rhu-pGSN to Mitigate Proinflammatory Responses to Decompression in Healthy SCUBA Divers
- phase3Efficacy and Safety of Alpha1-Proteinase Inhibitor (Human), Modified Process (Alpha-1 MP) in Subjects With Pulmonary Emphysema Due to Alpha1 Antitrypsin Deficiency (AATD)
- phase3A Study to Evaluate the Efficacy and Safety of CBL-514 Injection for Reducing Subcutaneous Fat
- phase2A Study to Evaluate the Efficacy and Safety of CBL-514 Compared to Placebo in Participants With Dercum's Disease Lipomas
- phase2Clinical Trial of Omalizumab for Allergen Sensitized and Exposed Individuals With COPD
- phase2A Study of BEBT-701 in Patients With Mild to Moderate Hypertension and Elevated Low-Density Lipoprotein Cholesterol（LDL-C）
News(10)
- Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing Recalled Sodium Chloride AmpulesBD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampulesfda_medwatch · 1mo ago
- Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate MatterROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product…fda_medwatch · 1mo ago
- Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Huons Sodium Chloride AmpulesAVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 1mo ago
- Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride InjectionOtsuka ICU Medical LLC is issuing a voluntary recall for one lot of 0.9% SODIUM CHLORIDE Injection, USP, 100mL single pack to the user level due to a potential mix-up. The affected lot of 0.9% SODI…fda_medwatch · 1mo ago
- Sodium Chloride Flush Recall: Spectra Medical Removes Sodium Chloride Injection USP AmpulesSpectra Medical Devices is removing Sodium Chloride Flush products that were manufactured by Huons Co,. Ltd.fda_medwatch · 1mo ago
- Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine AmpulesMedical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 1mo ago
- B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate MatterFOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Con…fda_medwatch · 1mo ago
- Early Alert: Convenience Kit Issue from AVID MedicalAVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 2mo ago
- Baxter Issues Voluntary Nationwide Recall for Two Lots of 0.9% Sodium Chloride Injection Due to Potential Presence of Particulate MatterFOR IMMEDIATE RELEASE – AUG. 25, 2026 – DEERFIELD, Ill., Baxter International Inc. (NYSE:BAX) is voluntarily recalling two lots of 0.9% Sodium Chloride Injection due to the potential presence of pa…fda_medwatch · 2mo ago
- Early Alert: Epidural Kit Issue from Medical Action IndustriesMedical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.fda_medwatch · 2mo ago
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