NDC 81643-9270 – Floxuridine

Floxuridine 500 mg/1 · Injection, Powder, Lyophilized, For Solution · Intra-arterial

Human Prescription Drug

Product NDC81643-9270

Product details

Brand name
Floxuridine
Generic name
Floxuridine
Labeler
JND Therapeutics, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intra-arterial
Marketing category
ANDA · ANDA075387
Marketed since
June 9, 2022
Listing expires
December 31, 2026
Pharmacologic class
Antimetabolite

Active ingredients

Uses, dosage, side effects and warnings for Floxuridine →

Package NDC codes (1)

Package NDCDescriptionSince
81643-9270-11 VIAL in 1 BOX, UNIT-DOSE (81643-9270-1) / 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALJun 9, 2022

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