NDC 43598-342 – Pralatrexate

Pralatrexate 20 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC43598-342

Product details

Brand name
Pralatrexate
Generic name
Pralatrexate
Labeler
Dr.Reddy's Laboratories Inc.,
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA206183
Marketed since
March 4, 2026
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pralatrexate →

Package NDC codes (1)

Package NDCDescriptionSince
43598-342-111 VIAL, SINGLE-DOSE in 1 CARTON (43598-342-11) / 1 mL in 1 VIAL, SINGLE-DOSEMar 4, 2026

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