NDC 0781-3519

Pemetrexed

Pemetrexed Disodium

Pemetrexed is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc.. The primary component is Pemetrexed Disodium.

Product ID0781-3519_4dd3bb2b-a3c3-4ede-bfdf-aeac922bcfde
NDC0781-3519
Product TypeHuman Prescription Drug
Proprietary NamePemetrexed
Generic NamePemetrexed Disodium
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2022-06-08
Marketing CategoryNDA /
Application NumberNDA214657
Labeler NameSandoz Inc.
Substance NamePEMETREXED DISODIUM
Active Ingredient Strength500 mg/20mL
Pharm ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0781-3519-90

1 VIAL in 1 CARTON (0781-3519-90) > 20 mL in 1 VIAL
Marketing Start Date2022-06-08
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

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.