Product Images Vancomycin Hydrochloride

This text provides information about Vancomycin Hydrochloride for Injection, USP. It includes details such as dosage, reconstitution instructions, storage conditions, manufacturer information, and precautions. The medication is supplied in 1.25g single-dose vials and is intended for intravenous use. It emphasizes the importance of reading the package insert before use and highlights the need for further dilution after reconstitution.*

This is information about a medication containing Vancomycin Hydrochloride. It provides details on dosage, administration, storage, and precautions. The text includes instructions to reconstitute the contents with sterile water for injection and emphasizes the necessity to dilute the solution further after reconstitution. It also specifies the storage conditions and shelf-life of the medication.*

Vancomycin Hydrochloride for Injection, USP is a sterile powder available in 10 x 750 mg single-dose vials. This medication is intended for intravenous use and must be further diluted after reconstitution. Each vial contains Vancomycin hydrochloride, USP equivalent to 750 mg. The usual adult dosage can be found in the package insert along with precautions and directions for use. Prior to reconstitution, it should be stored at 2°C to 25°C, and after reconstitution, it can be refrigerated for up to 14 days without significant loss of potency. This product is manufactured by Gland Pharma Limited in India.*

This is a description of a single-dose vial of Vancomycin Hydrochloride for Injection, USP. It is intended for intravenous use and must be further diluted after reconstitution. The product is in a sterile powder form and comes with an NDC code 68083-597-01. The text also includes some technical information and warnings related to the product's usage.*

This is a product label for a pharmaceutical item, potentially a vial containing 750 mg of medication for intravenous use. It is manufactured by Gland Pharma Limited in India. The text also includes details such as manufacturing location and authorization numbers. The product must be further diluted after reconstitution. If more information is needed, referring to the package insert is recommended.*