NDC 72789-030 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-030

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076796
Marketed since
March 26, 2004
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (2)

Package NDCDescriptionSince
72789-030-3030 TABLET in 1 BOTTLE, PLASTIC (72789-030-30)Dec 5, 2019
72789-030-6060 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)Dec 5, 2019

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