NDC 70771-1026 – Bumetanide

Bumetanide 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1026

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202900
Marketed since
May 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (5)

Package NDCDescriptionSince
70771-1026-01000 TABLET in 1 BOTTLE (70771-1026-0)May 1, 2018
70771-1026-1100 TABLET in 1 BOTTLE (70771-1026-1)May 1, 2018
70771-1026-330 TABLET in 1 BOTTLE (70771-1026-3)May 1, 2018
70771-1026-5500 TABLET in 1 BOTTLE (70771-1026-5)May 1, 2018
70771-1026-990 TABLET in 1 BOTTLE (70771-1026-9)May 1, 2018

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