pemetrexed
Generic: pemetrexed
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
pemetrexed disodium 100 mg/4mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-1045
Product ID
0409-1045_54cf7e63-ef81-4ced-b833-a73ad8980230
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA214218
Listing Expiration
2026-12-31
Marketing Start
2022-06-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04091045
Hyphenated Format
0409-1045
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
pemetrexed (source: ndc)
Generic Name
pemetrexed (source: ndc)
Application Number
NDA214218 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/4mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1045-01) / 4 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "54cf7e63-ef81-4ced-b833-a73ad8980230", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602363", "2602365", "2602366"], "spl_set_id": ["3ae68628-7ab0-4491-b3ae-6a8330b719c8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1045-01) / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-1045-01", "marketing_start_date": "20220627"}], "brand_name": "PEMETREXED", "product_id": "0409-1045_54cf7e63-ef81-4ced-b833-a73ad8980230", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0409-1045", "generic_name": "PEMETREXED", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PEMETREXED", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "100 mg/4mL"}], "application_number": "NDA214218", "marketing_category": "NDA", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}