Vancomycin Hydrochloride Injection, Powder, Lyophilized, For Solution
Product Images NDC 0409-4332

This is a sterile powder of Vancomycin hydrochloride for injection, which is only meant for intravenous administration. It is equivalent to 1 g Vancomycin but must be further diluted before use. The usual adult dose is 2 g daily, which should be diluted with 20 mL of sterile water for injection. The insert should be read before use for precautions and directions. It may contain HCI and/or NaOH for pH adjustment. After dilution, it should be refrigerated, while before reconstitution, it should be stored at 20 to 25°C (68 to 77°F). The product is lyophilized and distributed by Hospira Inc., Lake Forest, IL 60045 USA, under the brand name Novaplus.*

This text seems to be a mixture of different information and codes related to pharmaceuticals, specifically about Vancomycin Hydrochloride for Injection, USP. There are some NDC codes for different vials with 10 units of Vancomycin Hydrochloride. The text also mentions that the drug must be diluted before use and there is an insert that should be checked. This appears to be an incomplete version of some technical document or medical prescription.*

This is a description of a sterile powder medication called Vancomycin Hydrochloride for Injection, USP. One package of the medication contains an equivalent of 500mg vancomycin, and it's meant for intravenous use. The medication must be diluted with sterile water for injection before use, and the instructions on how to dilute are indicated on the package insert. The usual adult dosage is two daily. After dilution, the medication should be refrigerated. The medication is lyophilized, and its reconstitution should be done at a controlled room temperature. The manufacturer and distributor of the medication are Hospira, Inc. of Lake Forest, IL. There are some precautions and directions for use in the package insert that the user needs to read. The lot and expiration dates are also indicated on the package.*