NDC 0143-9270 – Floxuridine

Floxuridine 100 mg/mL · Injection, Powder, Lyophilized, For Solution · Intra-arterial

Human Prescription Drug

Product NDC0143-9270

Product details

Brand name
Floxuridine
Generic name
Floxuridine
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intra-arterial
Marketing category
ANDA · ANDA075387
Marketed since
February 15, 2018
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite

Active ingredients

Uses, dosage, side effects and warnings for Floxuridine →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9270-011 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01) / 5 mL in 1 VIALFeb 15, 2018

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