Pemetrexed 70069-0835

Generic: Pemetrexed Disodium

Product NDC

70069-0835

Manufacturer: Somerset Therapeutics Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: April 15, 2025
Listing Expires: December 31, 2026
Application: ANDA211899

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Active Ingredients

Ingredient	Strength
Pemetrexed Disodium Heptahydrate	500 mg/20mL

Drug Class

Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]

Packaging Options(1)

70069-0835-01

1 VIAL in 1 CARTON (70069-835-01) / 20 mL in 1 VIAL

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