NDC 60687-384 – Bumetanide

Bumetanide 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-384

Product details

Brand name
Bumetanide
Generic name
Bumetanide
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018225
Marketed since
August 2, 2018
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Bumetanide →

Package NDC codes (2)

Package NDCDescriptionSince
60687-384-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-384-01) / 1 TABLET in 1 BLISTER PACK (60687-384-11)Jul 13, 2020
60687-384-6550 BLISTER PACK in 1 CARTON (60687-384-65) / 1 TABLET in 1 BLISTER PACK (60687-384-11)Jun 5, 2023

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