NDC 55150-382 – Pemetrexed

Pemetrexed Disodium Hemipentahydrate 500 mg/20mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC55150-382

Product details

Brand name
Pemetrexed
Generic name
Pemetrexed
Labeler
Eugia US LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA214632
Marketed since
May 25, 2022
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pemetrexed →

Package NDC codes (1)

Package NDCDescriptionSince
55150-382-011 VIAL in 1 CARTON (55150-382-01) / 20 mL in 1 VIALMay 25, 2022

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