Contepo Injection, Powder, For Solution
Product Images NDC 71288-035

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Contepo (NDC 71288-035). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Figure 1 (Con0o 0000 01)

Figure 1 (Con0o 0000 01)
Chemical structure of fosfomycin disodium, showing the molecular arrangement including a phosphonate group and an epoxide ring, relevant to the active ingredient in Contepo injection powder for solution.*
FDA Label Image

Principal Display Panel (CONTEPO 6 grams per vial Container Label)

Principal Display Panel (CONTEPO 6 grams per vial Container Label)
Contepo (fosfomycin disodium) injection 6 grams per vial label for intravenous infusion only. The single-dose vial must be constituted and further diluted before use. The label includes storage instructions, manufacturer information for Meitheal Pharmaceuticals Inc., and barcode and lot/expiration placeholders.*
FDA Label Image

Principal Display Panel (CONTEPO 6 grams per vial Carton Label)

Principal Display Panel (CONTEPO 6 grams per vial Carton Label)
The image shows the flat carton label for Contepo (fosfomycin) injection, powder for solution, 6 grams per vial, intended for intravenous infusion. The label specifies the contents as 12 single-dose vials and includes handling instructions stating the product must be constituted and further diluted. The manufacturer is Meitheal Pharmaceuticals Inc., Chicago, IL.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.