Furosemide Injection, Solution
Product Images NDC 51662-1575
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 51662-1575). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Vial Label 1575 (51662 1575 1 Vial Labeling)
Furosemide Injection, USP is a sterile solution used for intravenous or intramuscular administration. It contains 100 mg of furosemide per 10 mL vial, with a concentration of 10 mg/mL. The solution is preservative-free and adjusted to isotonicity with sodium chloride. Its pH is regulated with sodium hydroxide and hydrochloric acid. The recommended dose is specified in the package insert. The solution should be stored at a controlled room temperature between 20°C to 25°C, protected from light. Discard the unused portion and do not use if discolored or the seal is ruptured. The lot number and expiration date are provided on the vial.*
Description (Description)
Hs (Hs)
The above text provides information on different variants of a product, identified by their respective product numbers and NDC codes. It also contains information on the strength of each variant, with the quantity of the active ingredient specified in milligrams per milliliter. The volume of each variant is also provided, along with the container type and color.*
Logo (Logo)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.