NDC 71335-2319 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2319

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216629
Marketed since
November 5, 2022
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2319-06 TABLET in 1 BOTTLE (71335-2319-0)Jan 4, 2024
71335-2319-130 TABLET in 1 BOTTLE (71335-2319-1)Jan 4, 2024
71335-2319-290 TABLET in 1 BOTTLE (71335-2319-2)Jan 4, 2024
71335-2319-360 TABLET in 1 BOTTLE (71335-2319-3)Jan 4, 2024
71335-2319-4100 TABLET in 1 BOTTLE (71335-2319-4)Jan 4, 2024
71335-2319-57 TABLET in 1 BOTTLE (71335-2319-5)Jan 4, 2024
71335-2319-628 TABLET in 1 BOTTLE (71335-2319-6)Jan 4, 2024
71335-2319-714 TABLET in 1 BOTTLE (71335-2319-7)Jan 4, 2024
71335-2319-810 TABLET in 1 BOTTLE (71335-2319-8)Jan 4, 2024
71335-2319-920 TABLET in 1 BOTTLE (71335-2319-9)Jan 4, 2024

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