pemetrexed

Generic: pemetrexed disodium

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pemetrexed
Generic Name pemetrexed disodium
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pemetrexed disodium hemipentahydrate 500 mg/20mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-261
Product ID 25021-261_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
folate analog metabolic inhibitor [epc] folic acid metabolism inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021261
Hyphenated Format 25021-261

Supplemental Identifiers

RxCUI
1728072 1728077
UNII
F4GSH45R4C

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 pemetrexed (source: ndc)
Generic Name pemetrexed disodium (source: ndc)
Application Number ANDA204890 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/20mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (25021-261-50) / 20 mL in 1 VIAL
source: ndc

Packages (1)

25021-261-50 1 VIAL in 1 CARTON (25021-261-50) / 20 mL in 1 VIAL

Ingredients (1)

pemetrexed disodium hemipentahydrate (500 mg/20mL)

Linked Drug Pages (1)

Pemetrexed ndc-match (0.9)

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 (25021-261-50)  / 20 mL in 1 VIAL", "package_ndc": "25021-261-50", "marketing_start_date": "20241215"}], "brand_name": "Pemetrexed", "product_id": "25021-261_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": "25021-261", "generic_name": "Pemetrexed Disodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "500 mg/20mL"}], "application_number": "ANDA204890", "marketing_category": "ANDA", "marketing_start_date": "20241215", "listing_expiration_date": "20261231"}