NDC 69315-116 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC69315-116

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
Leading Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077293
Marketed since
February 1, 2006
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (2)

Package NDCDescriptionSince
69315-116-01100 TABLET in 1 BOTTLE (69315-116-01)May 15, 2016
69315-116-101000 TABLET in 1 BOTTLE (69315-116-10)May 15, 2016

Recalls mentioning this NDC

Other Furosemide products