Alimta - 0002-7623-01 - (Pemetrexed disodium)

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Drug Information of Alimta

Product NDC: 0002-7623
Proprietary Name: Alimta
Non Proprietary Name: Pemetrexed disodium
Active Ingredient(s): 500    mg/20mL & 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: 0002-7623
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021462
Marketing Category: NDA
Start Marketing Date: 20040213

Package Information of Alimta

Package NDC: 0002-7623-01
Package Description: 1 VIAL in 1 CARTON (0002-7623-01) > 20 mL in 1 VIAL

NDC Information of Alimta

NDC Code 0002-7623-01
Proprietary Name Alimta
Package Description 1 VIAL in 1 CARTON (0002-7623-01) > 20 mL in 1 VIAL
Product NDC 0002-7623
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 20040213
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name PEMETREXED DISODIUM
Strength Number 500
Strength Unit mg/20mL
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Alimta


General Information