Package 0002-7623-01

Brand: alimta

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 0002-7623-01
Digits Only 0002762301
Product NDC 0002-7623
Description

1 VIAL in 1 CARTON (0002-7623-01) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2004-02-13
Brand alimta
Generic pemetrexed disodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3af0bc84-13d6-46aa-a4c0-c62410b73bc6", "openfda": {"unii": ["9T47E4OM16"], "rxcui": ["1728072", "1728075", "1728077", "1728079"], "spl_set_id": ["f5a860f3-37ec-429c-ae04-9c88d7c55c08"], "manufacturer_name": ["Eli Lilly and Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0002-7623-01)  / 20 mL in 1 VIAL", "package_ndc": "0002-7623-01", "marketing_start_date": "20040213"}], "brand_name": "Alimta", "product_id": "0002-7623_3af0bc84-13d6-46aa-a4c0-c62410b73bc6", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0002-7623", "generic_name": "Pemetrexed disodium", "labeler_name": "Eli Lilly and Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alimta", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEPTAHYDRATE", "strength": "500 mg/20mL"}], "application_number": "NDA021462", "marketing_category": "NDA", "marketing_start_date": "20040204", "listing_expiration_date": "20261231"}