NDC 68071-1708 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-1708

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077293
Marketed since
February 1, 2006
Listing expires
December 31, 2026
Pharmacologic class
Loop Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Furosemide →

Package NDC codes (1)

Package NDCDescriptionSince
68071-1708-1100 TABLET in 1 BOTTLE (68071-1708-1)Feb 6, 2019

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