NDC 68788-8870 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8870

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
Prefferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216629
Marketed since
April 30, 2025
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8870-1100 TABLET in 1 BOTTLE (68788-8870-1)Apr 30, 2025
68788-8870-330 TABLET in 1 BOTTLE (68788-8870-3)Apr 30, 2025
68788-8870-660 TABLET in 1 BOTTLE (68788-8870-6)Apr 30, 2025
68788-8870-990 TABLET in 1 BOTTLE (68788-8870-9)Apr 30, 2025

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