NDC 71335-2317 – Furosemide

Furosemide 40 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2317

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 (9)

Package NDCDescriptionSince
71335-2317-140 TABLET in 1 BOTTLE (71335-2317-1)Jan 2, 2024
71335-2317-230 TABLET in 1 BOTTLE (71335-2317-2)Jan 2, 2024
71335-2317-3100 TABLET in 1 BOTTLE (71335-2317-3)Jan 2, 2024
71335-2317-490 TABLET in 1 BOTTLE (71335-2317-4)Jan 2, 2024
71335-2317-560 TABLET in 1 BOTTLE (71335-2317-5)Jan 2, 2024
71335-2317-67 TABLET in 1 BOTTLE (71335-2317-6)Jan 2, 2024
71335-2317-714 TABLET in 1 BOTTLE (71335-2317-7)Jan 2, 2024
71335-2317-8180 TABLET in 1 BOTTLE (71335-2317-8)Jan 2, 2024
71335-2317-910 TABLET in 1 BOTTLE (71335-2317-9)Jan 2, 2024

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