NDC 68382-525 – Bumetanide

Bumetanide .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-525

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
Zydus Pharmaceuticals (USA) Inc.
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
68382-525-01100 TABLET in 1 BOTTLE (68382-525-01)May 1, 2018
68382-525-05500 TABLET in 1 BOTTLE (68382-525-05)May 1, 2018
68382-525-0630 TABLET in 1 BOTTLE (68382-525-06)May 1, 2018
68382-525-101000 TABLET in 1 BOTTLE (68382-525-10)May 1, 2018
68382-525-1690 TABLET in 1 BOTTLE (68382-525-16)May 1, 2018

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