Product Images Furosemide

This is a description of a medication called Furosemide which comes in a single-use vial of 10mL. The vial has a National Drug Code (NDC) of 0409-6102-20. The medication is an injection and contains 10mg of Furosemide and sodium chloride. It is intended for intravenous or intramuscular use. Hospira Inc. located in Lake Forest, IL is the manufacturer of this medication. The prescription or use of this medication after the expiring date is not advised. If the solution's discoloration is observed, it should not be used.*

This is a product description of different concentrations, unit of sale and packaging of medication. The product is sold in vials or bundled with syringes. The available concentrations are 20mg/2mL, 40mg/4mL and 100mg/10mL at 10mg/mL. There are different quantities of vials and syringes depending on the packaging listed with their corresponding National Drug Codes (NDC).*

This is a description of a medical product: Furosemide Injection, USP. The package comes in a single-use vial that contains 10 mL of the product. The manufacturer's package insert should be consulted for more information. The product is distributed by HF Acquisition Co., LLC based in Mukilteo, WA 98275.*

This is a description of a medication called Furosemide. It comes in a single-use vial of 10 ml and is only available through a prescription with the NDC code 0409-6102-20. It is important to not use it if the solution is discolored or contains particles. Each ml of the solution contains 10mg of Furosemide and sodium chloride. It is intended for intravenous or intramuscular use only. The product is distributed by Hospira Inc. based in Lake Forest, IL, USA. The lot and expiration number are also provided.*

This is a description of a 10 mL single-use vial manufactured by Hospira Inc. with the NDC code 0409-6102-20. It contains an intravenous or intramuscular medication called Furosemide, which comes in concentrations of 10 mg per milliliter. The solution may not be used if it is discolored or contains particulate. The medication is mixed with sodium chloride to achieve a sufficient concentration. The label includes a Lot/Exp. number in the format of HHE-HHH-AA DMMMYYYY.*