NDC 83831-112 – Pemetrexed Dipotassium

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

Human Prescription Drug

Product NDC83831-112

Product details

Brand name
Pemetrexed Dipotassium
Generic name
Pemetrexed dipotassium
Labeler
Avyxa Pharma, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA210661
Marketed since
January 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pemetrexed Dipotassium →

Package NDC codes (1)

Package NDCDescriptionSince
83831-112-011 VIAL in 1 CARTON (83831-112-01) / 20 mL in 1 VIALJan 1, 2025

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