Alimta - 0002-7640-01 - (Pemetrexed disodium)

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Drug Information of Alimta

Product NDC: 0002-7640
Proprietary Name: Alimta
Non Proprietary Name: Pemetrexed disodium
Active Ingredient(s): 100    mg/4mL & nbsp;   Pemetrexed disodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Alimta

Product NDC: 0002-7640
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021462
Marketing Category: NDA
Start Marketing Date: 20080115

Package Information of Alimta

Package NDC: 0002-7640-01
Package Description: 1 VIAL in 1 CARTON (0002-7640-01) > 4 mL in 1 VIAL

NDC Information of Alimta

NDC Code 0002-7640-01
Proprietary Name Alimta
Package Description 1 VIAL in 1 CARTON (0002-7640-01) > 4 mL in 1 VIAL
Product NDC 0002-7640
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pemetrexed disodium
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080115
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name PEMETREXED DISODIUM
Strength Number 100
Strength Unit mg/4mL
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Alimta


General Information