NDC 43598-342

Pralatrexate 20 mg per 1 mL injection

On the label: Dr. Reddy's Laboratories Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Dr.reddy's Laboratories LimitedVisakhapatnam, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action

Product details

Generic drug
Pralatrexate: every company that makes it
Form
injection, intravenous
Strength
20 mg per 1 mL
Approval
ANDA ANDA206183
On the market since
Mar 4, 2026
Package NDCs
43598-342-11
Official label
DailyMed (National Library of Medicine), updated Aug 31, 2025

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