pemetrexed

Generic: pemetrexed disodium

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pemetrexed disodium hemipentahydrate 500 mg/20mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-539
Product ID 68001-539_eed98f1e-acdf-28da-e053-2a95a90a046c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204890
Listing Expiration 2026-12-31
Marketing Start 2022-06-24

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 68001539
Hyphenated Format 68001-539

Supplemental Identifiers

RxCUI
1728072 1728077
UPC
0368001539418 0368001538411
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 (68001-539-41) / 20 mL in 1 VIAL
source: ndc

Packages (1)

68001-539-41 1 VIAL in 1 CARTON (68001-539-41) / 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": "eed98f1e-acdf-28da-e053-2a95a90a046c", "openfda": {"upc": ["0368001539418", "0368001538411"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["c9f34c00-1176-4f44-8cff-bae5bdc0c40f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-539-41)  / 20 mL in 1 VIAL", "package_ndc": "68001-539-41", "marketing_start_date": "20220624"}], "brand_name": "Pemetrexed", "product_id": "68001-539_eed98f1e-acdf-28da-e053-2a95a90a046c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-539", "generic_name": "Pemetrexed disodium", "labeler_name": "BluePoint Laboratories", "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": "20220624", "listing_expiration_date": "20261231"}