NDC 68001-549

Pemetrexed

Pemetrexed

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

Product ID68001-549_e231cb1a-cd9f-5036-e053-2a95a90ae05a
NDC68001-549
Product TypeHuman Prescription Drug
Proprietary NamePemetrexed
Generic NamePemetrexed
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-06-27
Marketing CategoryANDA /
Application NumberANDA203485
Labeler NameBluePoint Laboratories
Substance NamePEMETREXED DISODIUM HEMIPENTAHYDRATE
Active Ingredient Strength1 g/40mL
Pharm ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 68001-549-41

1 VIAL in 1 CARTON (68001-549-41) > 40 mL in 1 VIAL
Marketing Start Date2022-06-27
NDC Exclude FlagN
Sample Package?N

Drug Details

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

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
50742-340PemetrexedPemetrexed disodium
50742-341PemetrexedPemetrexed disodium
55150-381PemetrexedPemetrexed
55150-382PemetrexedPemetrexed
42367-531Pemfexypemetrexed
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