NDC 65219-552 – Pralatrexate

Pralatrexate 40 mg/2mL · Injection · Intravenous

Human Prescription Drug

Product NDC65219-552

Product details

Brand name
Pralatrexate
Generic name
Pralatrexate
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection
Route
Intravenous
Marketing category
NDA AUTHORIZED GENERIC · NDA022468
Marketed since
November 15, 2022
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pralatrexate →

Package NDC codes (1)

Package NDCDescriptionSince
65219-552-021 VIAL, SINGLE-DOSE in 1 CARTON (65219-552-02) / 2 mL in 1 VIAL, SINGLE-DOSENov 15, 2022

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