pemetrexed
Generic: pemetrexed disodium
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed disodium
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
pemetrexed disodium hemipentahydrate 100 mg/4.2mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-260
Product ID
25021-260_f9386c39-eee1-4407-91b7-f55bc710897a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204890
Listing Expiration
2026-12-31
Marketing Start
2024-12-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021260
Hyphenated Format
25021-260
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
ANDA204890 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/4.2mL
Packaging
- 1 VIAL in 1 CARTON (25021-260-10) / 4.2 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": "f9386c39-eee1-4407-91b7-f55bc710897a", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["fa8f1f52-3f05-4ae8-bfec-7f0a029e6825"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-260-10) / 4.2 mL in 1 VIAL", "package_ndc": "25021-260-10", "marketing_start_date": "20241215"}], "brand_name": "Pemetrexed", "product_id": "25021-260_f9386c39-eee1-4407-91b7-f55bc710897a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "25021-260", "generic_name": "Pemetrexed Disodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4.2mL"}], "application_number": "ANDA204890", "marketing_category": "ANDA", "marketing_start_date": "20241215", "listing_expiration_date": "20261231"}