Furosemide Injection, Solution
Product Images NDC 71872-7308

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 71872-7308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

7308.pdp (7308)

This is a description of Furosemide Injection, USP in a 100 mg/10 mL single-dose vial for intravenous or intramuscular use. Each mL contains 10 mg of Furosemide, USP along with Water for Injection, USP, Sodium Chloride, USP, Sodium Hydroxide, NF, and Hydrochloric Acid, NF for pH adjustment. It includes warnings to discard unused portions, use only clear and colorless solution, and store between 20°C to 25°C. The manufacturing information indicates Emcure Pharmaceuticals Ltd., India, and repackaging by Medical Purchasing Solutions in Scottsdale, AZ. For more details, the package insert should be referenced.*

FDA Label Image

73081.pdp (73081)

This text is a label for Furosemide Injection, USP with a strength of 100 mg per 10 mL vial. The medication is meant for intravenous or intramuscular use and should only be used if the solution is clear and colorless. It needs to be protected from light and stored between 20°C to 25°C (68°F to 77°F). The manufacturer is Maiva Pharma Private Limited in Tamilnadu, India, and it is made for Avet Pharmaceuticals Inc. The label also includes a code number and references to package insert instructions.*

FDA Label Image

Logo (Avetlogo)

FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.