alimta
Generic: pemetrexed disodium
Labeler: eli lilly and companyDrug Facts
Product Profile
Brand Name
alimta
Generic Name
pemetrexed disodium
Labeler
eli lilly and company
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
pemetrexed disodium heptahydrate 500 mg/20mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00027623
Hyphenated Format
0002-7623
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 500 mg/20mL
Packaging
- 1 VIAL in 1 CARTON (0002-7623-01) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
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"}