Country: United States
Language: English
Source: NLM (National Library of Medicine)
SUCCINYLCHOLINE CHLORIDE (UNII: I9L0DDD30I) (SUCCINYLCHOLINE - UNII:J2R869A8YF)
Cantrell Drug Company
SUCCINYLCHOLINE CHLORIDE
SUCCINYLCHOLINE CHLORIDE 20 mg in 1 mL
PRESCRIPTION DRUG
unapproved drug other
SUCCINYLCHOLINE CHLORIDE- SUCCINYLCHOLINE CHLORIDE INJECTION, SOLUTION CANTRELL DRUG COMPANY _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- SUCCINYLCHOLINE CHLORIDE 20 MG/ML INJECTION SOLUTION 10 ML SYRINGE • WARNINGS AND PRECAUTIONS Outsourced Compounded Drug. Not for Resale. Hospital/Office Use Only. WARNING: PARALYZING AGENT. CAUSES RESPIRATORY ARREST. SUCCINYLCHOLINE SHOULD BE USED ONLY BY THOSE SKILLED IN THE MANAGEMENT OF ARTIFICIAL RESPIRATION AND ONLY WHEN FACILITIES ARE INSTANTLY AVAILABLE FOR TRACHEAL INTUBATION AND FOR PROVIDING ADEQUATE VENTILATION OF THE PATIENT, INCLUDING THE ADMINISTRATION OF OXYGEN UNDER POSITIVE PRESSURE AND THE ELIMINATION OF CARBON DIOXIDE. THE CLINICIAN MUST BE PREPARED TO ASSIST OR CONTROL RESPIRATION. • ADVERSE EVENTS To facilitate Adverse Event Reporting: www.fda.gov/medwatch or 1-800-FDA-1088. • HOW SUPPLIED Succinylcholine Chloride is supplied as a sterile, isotonic, nonpyrogenic solution that is clear, colorless in a 10 mL Single-Dose Syringe. This product is Preservative-Free and Latex-Free. • INGREDIENTS Each 1 mL contains 20 mg Succinylcholine Chloride and made isotonic with 4.36 mg Sodium Chloride, USP, in Sterile Water for Injection. The aqueous solution is adjusted to a pH of 3.5 with hydrochloric acid and/or sodium hydroxide, if necessary. • STORAGE AND HANDLING Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]. • DOSAGE AND ADMINISTRATION. FOR INTRAVENOUS USE. PRESERVATIVE-FREE INJECTION SOLUTION. The dosage of succinylcholine should be individualized and should always be determined by the clinician after careful assessment of the patient. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Solutions that are discolored and/or contain particulate matter should not be use Read the complete document