NDC 70121-2461 – Pemrydi Rtu

Pemetrexed Disodium Hemipentahydrate 500 mg/50mL · Injection · Intravenous

Human Prescription Drug 2 recalls

Product NDC70121-2461

Product details

Brand name
Pemrydi Rtu
Generic name
Pemetrexed disodium
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection
Route
Intravenous
Marketing category
NDA · NDA215179
Marketed since
June 6, 2023
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pemrydi Rtu →

Package NDC codes (1)

Package NDCDescriptionSince
70121-2461-11 VIAL in 1 CARTON (70121-2461-1) / 50 mL in 1 VIALJun 6, 2023

Recalls mentioning this NDC

Other Pemrydi Rtu products