NDC 30698-631 – Bumex

Bumetanide 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC30698-631

Product details

Brand name
Bumex
Generic name
Bumetanide
Labeler
Validus Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA018225
Marketed since
February 28, 1983
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumex →

Package NDC codes (2)

Package NDCDescriptionSince
30698-631-01100 TABLET in 1 BOTTLE (30698-631-01)Feb 28, 1983
30698-631-05500 TABLET in 1 BOTTLE (30698-631-05)Jan 17, 2024

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