"The U.S. Food and Drug Administration today approved the MemoryShape Breast Implant to increase breast size (augmentation) for use in women at least 22 years old and to rebuild breast tissue (reconstruction) in women of any age. The MemoryShape B"...
(sodium lactate (sodium lactate injection in aviva) injection in aviva) Injection USP
Sodium Lactate Injection, USP, 50 mEq (5 mEq/mL) is a sterile, nonpyrogenic, concentrated solution of sodium lactate (sodium lactate injection in aviva) in Water for Injection for additive use only after dilution by intravenous route as an electrolyte replen-isher and systemic alkalizer. It should not be administered undiluted.
Sodium lactate (sodium lactate injection in aviva) is chemically designated as propanoic acid, 2-hydroxy-,monosodium salt and has the following structural formula:
A 60% aqueous solution is miscible in water.
Each mLcontains: Sodium lactate (sodium lactate injection in aviva) anhydrous 560 mg (5 mEq each of Na+ and lactate anion); Water for Injection q.s. Hydrochloric acid and/ or sodium hydroxide for pH adjustment.
The solution contains no bacteriostat, antimicrobial agent or added buffer. The osmolar concentration is 10 mOsmol/mL (calc.). When diluted with Sterile Water for Injection to make a 1/6 molar solution, the pH of sodium lactate (sodium lactate injection in aviva) solution lies between 6.0 and 7.3.
Last reviewed on RxList: 1/16/2009
This monograph has been modified to include the generic and brand name in many instances.
Additional Sodium Lactate Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Find out what women really need.