pemetrexed

Generic: pemetrexed disodium

Labeler: apotex corp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pemetrexed disodium 750 mg/30mL

Manufacturer
Apotex Corp

Identifiers & Regulatory

Product NDC 60505-6068
Product ID 60505-6068_bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209851
Marketing Start 2022-05-25
Marketing End 2026-06-30

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 605056068
Hyphenated Format 60505-6068

Supplemental Identifiers

RxCUI
2602136
UNII
2PKU919BA9

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 ANDA209851 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 750 mg/30mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (60505-6068-0) / 30 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

pemetrexed disodium (750 mg/30mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602136"], "spl_set_id": ["2e86f231-e0c7-2d43-2920-6c42d2469d11"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (60505-6068-0)  / 30 mL in 1 VIAL", "package_ndc": "60505-6068-0", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "60505-6068_bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "60505-6068", "generic_name": "Pemetrexed disodium", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "750 mg/30mL"}], "application_number": "ANDA209851", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}