NDC 70860-202

Pemetrexed

Pemetrexed Disodium

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

Product ID70860-202_83808721-efdf-404b-bc3a-1a1b8eb57445
NDC70860-202
Product TypeHuman Prescription Drug
Proprietary NamePemetrexed
Generic NamePemetrexed Disodium
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-05-25
Marketing CategoryANDA /
Application NumberANDA207352
Labeler NameAthenex Pharmaceutical Division, LLC.
Substance NamePEMETREXED DISODIUM HEMIPENTAHYDRATE
Active Ingredient Strength100 mg/4.2mL
Pharm ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 70860-202-10

1 VIAL, SINGLE-DOSE in 1 CARTON (70860-202-10) > 4.2 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2022-05-25
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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