NDC 0409-6102 – Furosemide

Furosemide 10 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug 2 recalls

Product NDC0409-6102

Product details

Brand name
Furosemide
Generic name
furosemide
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
NDA · NDA018667
Marketed since
November 19, 2013
Listing expires
December 31, 2027
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (6)

Package NDCDescriptionSince
0409-6102-0225 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-02) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-6102-19)Feb 28, 2005
0409-6102-0425 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-04) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-18)Feb 28, 2005
0409-6102-1025 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6102-20)Mar 31, 2005
0409-6102-2525 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-25) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-6102-35)Nov 19, 2013
0409-6102-2625 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-26) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-36)Nov 19, 2013
0409-6102-2725 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-27) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6102-37)Nov 19, 2013

Recalls mentioning this NDC

Other Furosemide products