Product Images Meropenem And Sodium Chloride

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 9 images provide visual information about the product associated with Meropenem And Sodium Chloride NDC 0264-3185 by B. Braun Medical Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Diagram 1 - meropenem in duplex 1

Diagram 1 - meropenem in duplex 1

Diagram 2 - meropenem in duplex 2

Diagram 2 - meropenem in duplex 2

Diagram 3 - meropenem in duplex 3

Diagram 3 - meropenem in duplex 3

Diagram 4 - meropenem in duplex 4

Diagram 4 - meropenem in duplex 4

Diagram 5 - meropenem in duplex 5

Diagram 5 - meropenem in duplex 5

structural formula - meropenem in duplex 6

structural formula - meropenem in duplex 6

500 mg 50mL container label - meropenem in duplex 7

500 mg 50mL container label - meropenem in duplex 7

1g 50mL container label - meropenem in duplex 8

1g 50mL container label - meropenem in duplex 8

Meropenem for injection is an antibiotic drug that is used for intravenous infusion only. The drug comes in a DUPLEX container which must be used only after mixing the contents of both chambers. Once reconstituted, each 50mL single-dose unit contains sterile meropenem trihydrate USP with a total sodium content of 290.2 mg. Prior to reconstitution, the drug must be stored at 20°C-25°C, and after reconstitution, the solution must be clear and free from particulate matter before use. The product must be used within seven days of removing the foil strip, and not beyond the labeled expiration date. The container must be protected from light after removal of the foil strip. The drug has not been manufactured with natural rubber latex, PVC, or DEHP.*

Drug Chamber - meropenem in duplex 9

Drug Chamber - meropenem in duplex 9

The text is a set of instructions related to a drug chamber. It suggests discarding the unit if the foil strip is damaged and visually inspecting the drug before reconstitution. The package insert should be referred to for detailed directions on reconstitution and administration. The text includes a reference number "I3" and a product code "yar001-485".*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.