pemetrexed
Generic: pemetrexed disodium
Labeler: sandoz inc.Drug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed disodium
Labeler
sandoz inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
pemetrexed disodium 100 mg/4mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3518
Product ID
0781-3518_764ab64b-c642-4314-83a9-efee79fe83a3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA214657
Listing Expiration
2026-12-31
Marketing Start
2022-06-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813518
Hyphenated Format
0781-3518
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 disodium (source: ndc)
Application Number
NDA214657 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/4mL
Packaging
- 1 VIAL in 1 CARTON (0781-3518-76) / 4 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": "764ab64b-c642-4314-83a9-efee79fe83a3", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602363", "2602365", "2602366"], "spl_set_id": ["7ac04ab7-7f8c-46ce-ab56-a7a08cd02ab3"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-3518-76) / 4 mL in 1 VIAL", "package_ndc": "0781-3518-76", "marketing_start_date": "20220608"}], "brand_name": "Pemetrexed", "product_id": "0781-3518_764ab64b-c642-4314-83a9-efee79fe83a3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0781-3518", "generic_name": "Pemetrexed disodium", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "100 mg/4mL"}], "application_number": "NDA214657", "marketing_category": "NDA", "marketing_start_date": "20220608", "listing_expiration_date": "20261231"}