NDC 51672-4118 – Fluorouracil

Fluorouracil 50 mg/g · Cream · Topical

Human Prescription Drug 1 recall

Product NDC51672-4118

Product details

Brand name
Fluorouracil
Generic name
Fluorouracil
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA090368
Marketed since
March 5, 2010
Listing expires
December 31, 2027
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Fluorouracil →

Package NDC codes (3)

Package NDCDescriptionSince
51672-4118-21 TUBE in 1 CARTON (51672-4118-2) / 25 g in 1 TUBEMar 17, 2017
51672-4118-55 g in 1 TUBE (51672-4118-5)Mar 17, 2017
51672-4118-61 TUBE in 1 CARTON (51672-4118-6) / 40 g in 1 TUBEMar 17, 2017

Recalls mentioning this NDC

Other Fluorouracil products