alimta

Generic: pemetrexed disodium

Labeler: eli lilly and company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name alimta
Generic Name pemetrexed disodium
Labeler eli lilly and company
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pemetrexed disodium heptahydrate 500 mg/20mL

Manufacturer
Eli Lilly and Company

Identifiers & Regulatory

Product NDC 0002-7623
Product ID 0002-7623_3af0bc84-13d6-46aa-a4c0-c62410b73bc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021462
Listing Expiration 2026-12-31
Marketing Start 2004-02-04

Pharmacologic Class

Classes
folate analog metabolic inhibitor [epc] folic acid metabolism inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00027623
Hyphenated Format 0002-7623

Supplemental Identifiers

RxCUI
1728072 1728075 1728077 1728079
UNII
9T47E4OM16

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name alimta (source: ndc)
Generic Name pemetrexed disodium (source: ndc)
Application Number NDA021462 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/20mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (0002-7623-01) / 20 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

pemetrexed disodium heptahydrate (500 mg/20mL)

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"}