NDC 70069-835 – Pemetrexed

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

Human Prescription Drug

Product NDC70069-835

Product details

Brand name
Pemetrexed
Generic name
Pemetrexed disodium
Labeler
Somerset Therapeutics LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA211899
Marketed since
April 15, 2025
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
70069-835-011 VIAL in 1 CARTON (70069-835-01) / 20 mL in 1 VIALApr 15, 2025

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