NDC 71335-0384 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0384

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
Bryant Ranch Prepack
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 (9)

Package NDCDescriptionSince
71335-0384-130 TABLET in 1 BOTTLE (71335-0384-1)Feb 9, 2022
71335-0384-290 TABLET in 1 BOTTLE (71335-0384-2)Feb 9, 2022
71335-0384-360 TABLET in 1 BOTTLE (71335-0384-3)Feb 9, 2022
71335-0384-4100 TABLET in 1 BOTTLE (71335-0384-4)Feb 9, 2022
71335-0384-57 TABLET in 1 BOTTLE (71335-0384-5)Feb 9, 2022
71335-0384-628 TABLET in 1 BOTTLE (71335-0384-6)Feb 9, 2022
71335-0384-714 TABLET in 1 BOTTLE (71335-0384-7)Feb 9, 2022
71335-0384-810 TABLET in 1 BOTTLE (71335-0384-8)Feb 9, 2022
71335-0384-920 TABLET in 1 BOTTLE (71335-0384-9)Feb 9, 2022

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