Floxuridine 500 mg / 1 Injection 1 Vial

Core reference details for licensed healthcare facility review and verification.

Floxuridine NDC Family 81643-9270 Floxuridine 500 mg / 1

NDC 11	81643-9270-01
Product NDC	81643-9270
Generic Drug Name	Floxuridine
Brand Name	Floxuridine
Manufacturer	JND Therapeutics, Inc.
Strength	500 mg / 1
Dosage Form	Injection
Drug Type	Intra-Arterial
Package Quantity	1 Vial
Package Description	1 VIAL in 1 BOX, UNIT-DOSE (81643-9270-1) / 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Active Ingredients	Floxuridine
Marketing Category	ANDA

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Core NDC snapshot

Floxuridine 500 mg / 1 Injection is tracked under NDC 81643-9270-01 and rolls up into product family 81643-9270. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 1 Vial.
Manufacturer: JND Therapeutics, Inc..
Dosage form: Injection.
Family size: 1 indexed presentation.

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Official references

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Floxuridine 500 mg / 1 Injection 1 Vial, NDC 81643-9270-01, is a JND Therapeutics, Inc. 500 mg / 1 injection presentation packaged as 1 Vial.

NDC search formats

Canonical NDC 11: 81643-9270-01
Digits-only NDC 11: 81643927001
Possible 10-digit display format: 81643-9270-1 (8164392701)

Helpful product links

Search by brand name: Floxuridine
NDC 11: 81643-9270-01
Product family NDC: 81643-9270
VA classification code: AN300
VA classification code description: ANTINEOPLASTICS,ANTIMETABOLITES
CMOP ID: F0415
VUID: 4027873