Esmolol Hydrochloride Injection
Product Images NDC 10019-120

This is a description for a hydrochloride injection in a ready-to-use vial that contains 100mg/10mL of hydrochloride (10 mg/ml). The injection is iso-osmotic and is safe to be used intravenously. It does not contain preservatives and unused portions should be discarded. The NDC number is 10018-120-39. There are also contact numbers for AORI and Desrad provided.*

This is a description for Esmolol Hydrochloride a drug manufactured for Baxler Healthcare Corporation. It is a clear, ready-to-use solution for intravenous use with each mL containing 10 mg of Esmolol Hydrochloride, USP, and 5.3 mg of Sodium Chloride, USP in Water for Injection, USP. The solution is buffered with Sodium Acetate Trihydrate, USP, and Glacial Acetic Acid, USP. Sodium Hydroxide and/or Hydrochloric Hydrochloride Injection Acid has been included to stabilize the pH of the solution. The drug is stored at 25°C (77°F) and should not be used if discolored or if a precipitate is noted. The drug comes in 25 x 10 mL Ready-to-use Vials, and each vial is for single use only. The solution is Iso-Osmotic, contains no preservatives, and contact with alkalies should be avoided. The packaging insert should be consulted for more information on dosage, administration, and storage.*

Each pack contains four ready-to-use vials of Esmolol Hydrochloride Injection with a strength of 100mg/10mL (10mg/mL) and a volume of 10mL per vial. The product is to be stored at 25°C (77°F) with an expiration date of December 2099 and a lot number of ABCDE12345. The product is manufactured for Baxter Healthcare Corporation in Deerfield, IL. If the last line of the text is not a typo, it is unrelated to the description of the product and might be gibberish or encrypted language.*