NDC 50742-340

Pemetrexed

Pemetrexed Disodium

Pemetrexed is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Ingenus Pharmaceuticals, Llc. The primary component is Pemetrexed Disodium Hemipentahydrate.

Product ID50742-340_12d4ace5-4ce2-469a-9a42-380a68328670
NDC50742-340
Product TypeHuman Prescription Drug
Proprietary NamePemetrexed
Generic NamePemetrexed Disodium
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-05-24
Marketing CategoryANDA /
Application NumberANDA204890
Labeler NameIngenus Pharmaceuticals, LLC
Substance NamePEMETREXED DISODIUM HEMIPENTAHYDRATE
Active Ingredient Strength100 mg/4mL
Pharm ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 50742-340-01

1 VIAL in 1 CARTON (50742-340-01) > 4 mL in 1 VIAL
Marketing Start Date2022-05-24
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Pemetrexed" or generic name "Pemetrexed Disodium"

NDCBrand NameGeneric Name
0338-0720PEMETREXEDPEMETREXED
0338-0722PEMETREXEDPEMETREXED
0409-1045PEMETREXEDPEMETREXED
0409-1060PemetrexedPemetrexed
0409-1061PemetrexedPemetrexed
0409-1062PemetrexedPemetrexed
0409-2188PEMETREXEDPEMETREXED
0409-3532PEMETREXEDPEMETREXED
0480-4514PemetrexedPemetrexed
0480-4515PemetrexedPemetrexed
0480-4516PemetrexedPemetrexed
0781-3518PemetrexedPemetrexed disodium
0781-3519PemetrexedPemetrexed disodium
0781-3520PemetrexedPemetrexed disodium
16729-229PemetrexedPemetrexed
16729-230PemetrexedPemetrexed
16729-244PemetrexedPemetrexed
16729-522PemetrexedPemetrexed disodium
0002-7623AlimtaPemetrexed disodium
0002-7640AlimtaPemetrexed disodium

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