NDC 43063-702 – Furosemide

Furosemide 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC43063-702

Product details

Brand name
Furosemide
Generic name
Furosemide
Labeler
PD-Rx 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 (5)

Package NDCDescriptionSince
43063-702-2121 TABLET in 1 BOTTLE, PLASTIC (43063-702-21)Jan 31, 2017
43063-702-3030 TABLET in 1 BOTTLE, PLASTIC (43063-702-30)Sep 29, 2016
43063-702-6060 TABLET in 1 BOTTLE, PLASTIC (43063-702-60)Aug 10, 2016
43063-702-791 TABLET in 1 BOTTLE, PLASTIC (43063-702-79)Feb 21, 2017
43063-702-9090 TABLET in 1 BOTTLE, PLASTIC (43063-702-90)Jan 4, 2017

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