Furosemide Injection, Solution
Product Images NDC 68083-434

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 68083-434). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

10-ml-vial (10 mL Vial)

Label for Furosemide Injection, USP 100 mg/10 mL (10 mg/mL) solution for injection in a 10 mL single dose vial by Gland Pharma Limited. The label states it is preservative free and intended for intravenous or intramuscular use. It includes a barcode, manufacturing details, and usage warnings.*

FDA Label Image

10ml-carton-25s-pack (10ml Carton 25s Pack)

Packaging label for Furosemide Injection, USP 100 mg/10 mL (10 mg/mL) by Gland Pharma Limited. The label indicates a preservative-free solution for intravenous or intramuscular use, supplied as 25 single dose vials of 10 mL each. Storage instructions and manufacturing details are included on the label.*

FDA Label Image

10ml-carton-5s-pack (10ml Carton 5s Pack)

Furosemide Injection, USP 10 mg/mL (100 mg/10 mL) preservative-free injection solution for intravenous or intramuscular use. The label depicts a package containing 5 single-dose 10 mL vials. The product is manufactured by Gland Pharma Limited in India. Directions and storage conditions are noted on the label.*

FDA Label Image

2-ml-vial (2 mL Vial)

Label for Furosemide Injection, USP 20 mg/2 mL (10 mg/mL) single dose vial, preservative free. Indicated for intravenous or intramuscular use. Manufactured by Gland Pharma Limited. Includes storage warnings and barcode on a white label with black and red text.*

FDA Label Image

2ml-carton-25s-pack (2ml Carton 25s Pack)

Packaging label for Furosemide Injection, USP 20 mg/2 mL (10 mg/mL) solution for injection. The label indicates use for intravenous or intramuscular administration. It contains 25 single-dose vials of 2 mL each, preservative free, manufactured by Gland Pharma Limited. The label includes warnings, storage instructions, and a barcode.*

FDA Label Image

2ml-carton-5s-pack (2ml Carton 5s Pack)

Furosemide Injection, USP 20 mg/2 mL (10 mg/mL) solution for injection in single dose vials. The label states it is for intravenous or intramuscular use and preservative free. The package contains 5 vials of 2 mL each. Manufactured by Gland Pharma Limited.*

FDA Label Image

4-ml-vial (4 mL Vial)

Label for Furosemide Injection, USP 40 mg/4 mL (10 mg/mL) injection solution by Gland Pharma Limited. This single-dose vial contains a preservative-free solution for intravenous or intramuscular use. The label includes formulation details, storage instructions, barcode, and manufacturer information.*

FDA Label Image

4ml-carton-25s-pack (4ml Carton 25s Pack)

Packaging label for Furosemide Injection USP 40 mg/4 mL (10 mg/mL) solution. The injection is for intravenous or intramuscular use, preservative free, supplied in 25 x 4 mL single dose vials. The product is manufactured by Gland Pharma Limited, with detailed storage and usage instructions noted on the label.*

FDA Label Image

4ml-carton-5s-pack (4ml Carton 5s Pack)

Furosemide Injection, USP 40 mg/4 mL (10 mg/mL) injection solution carton for intravenous or intramuscular use. The label indicates preservative-free single-dose vials, 5 vials per package. Manufactured by Gland Pharma Limited, India. Includes storage, usage, and warning information.*

FDA Label Image

Structure (Structure)

Chemical structure of the active ingredient Furosemide, showing its molecular components including a chlorinated benzene ring, sulfonamide group, carboxylic acid, and a furan ring.*

* 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.