NDC 71335-0842 – Furosemide

Furosemide 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0842

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076796
Marketed since
March 26, 2004
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
71335-0842-140 TABLET in 1 BOTTLE (71335-0842-1)May 31, 2018
71335-0842-230 TABLET in 1 BOTTLE (71335-0842-2)May 31, 2018
71335-0842-3100 TABLET in 1 BOTTLE (71335-0842-3)May 31, 2018
71335-0842-490 TABLET in 1 BOTTLE (71335-0842-4)May 31, 2018
71335-0842-560 TABLET in 1 BOTTLE (71335-0842-5)May 31, 2018
71335-0842-67 TABLET in 1 BOTTLE (71335-0842-6)May 31, 2018
71335-0842-714 TABLET in 1 BOTTLE (71335-0842-7)May 31, 2018
71335-0842-8180 TABLET in 1 BOTTLE (71335-0842-8)May 31, 2018
71335-0842-910 TABLET in 1 BOTTLE (71335-0842-9)May 31, 2018

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