Furosemide Injection, Solution
Product Images NDC 71288-203

7 FDA label images from Meitheal Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Furosemide (NDC 71288-203). 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.

FDA Label Image

Structural Formula (Fur05 0001 01)

Structural Formula (Fur05 0001 01)
Chemical structure of Furosemide, illustrating the molecular arrangement of its atoms including a benzene ring with substitutions, a carboxyl group, a sulfonamide group, a chlorine atom, an amine side chain, and a furan ring.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 20 mg Per 2 mL Container Label (Fur05 0001 02 V3)

Principal Display Panel – Furosemide Injection, Usp 20 mg Per 2 mL Container Label (Fur05 0001 02 V3)
Furosemide Injection, USP 20 mg per 2 mL (10 mg per mL) in a 2 mL single-dose vial. Labeled for intravenous or intramuscular use, manufactured for Meitheal Pharmaceuticals Inc. The label includes storage instructions to protect from light and store at 20° to 25°C (68° to 77°F). The product is a clear, colorless solution with warnings for discard of unused portion.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 20 mg Per 2 mL Carton (Fur05 0001 03 V3)

Principal Display Panel – Furosemide Injection, Usp 20 mg Per 2 mL Carton (Fur05 0001 03 V3)
Packaging label for Furosemide Injection, USP, 20 mg per 2 mL (10 mg per mL) in solution form. The product is supplied in a carton containing 25 single-dose vials of 2 mL each for intravenous or intramuscular use. The labeler is Meitheal Pharmaceuticals Inc., and the product NDC is 71288-203.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 40 mg Per 4 mL Container Label (Fur05 0001 04 V3)

Principal Display Panel – Furosemide Injection, Usp 40 mg Per 4 mL Container Label (Fur05 0001 04 V3)
Label for Furosemide Injection, USP 40 mg per 4 mL (10 mg per mL) single-dose vial for intravenous or intramuscular use. Contains 10 mg/mL Furosemide with other ingredients listed. Label includes usage warnings, storage instructions, lot, and expiration date fields, and states it is manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, made in China, product of India.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 40 mg Per 4 mL Carton (Fur05 0001 05 V4)

Principal Display Panel – Furosemide Injection, Usp 40 mg Per 4 mL Carton (Fur05 0001 05 V4)
Packaging label for Furosemide Injection, USP 40 mg per 4 mL (10 mg per mL) by Meitheal Pharmaceuticals Inc. It is an injection solution for intramuscular or intravenous use, contained in a box holding 25 single-dose vials of 4 mL each. The label includes dosage strength, administration routes, storage instructions, and manufacturer details.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 100 mg Per 10 mL Container Label (Fur05 0001 06 V3)

Principal Display Panel – Furosemide Injection, Usp 100 mg Per 10 mL Container Label (Fur05 0001 06 V3)
Label for Furosemide Injection, USP 10 mg/mL (100 mg per 10 mL) single-dose vial by Meitheal Pharmaceuticals Inc. The label states the product is for intravenous or intramuscular use. It includes storage instructions, warnings, and manufacturer information showing production in China and India. The NDC number 71288-203-10 is visible.*
FDA Label Image

Principal Display Panel – Furosemide Injection, Usp 100 mg Per 10 mL Carton Label (Fur05 0001 07 V4)

Principal Display Panel – Furosemide Injection, Usp 100 mg Per 10 mL Carton Label (Fur05 0001 07 V4)
Packaging label for Furosemide Injection, USP 10 mg/mL (100 mg per 10 mL) by Meitheal Pharmaceuticals Inc. The label indicates 25 single-dose vials of 10 mL each, for intravenous or intramuscular use. The product NDC is 71288-203-11. The label includes dosage strength, usage route, Rx only designation, and manufacturer logo.*

* 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.