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 1000 mg/40mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-546
Product ID 68001-546_fa3ecbbb-86e3-6fca-e053-6394a90a56d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209085
Listing Expiration 2026-12-31
Marketing Start 2023-02-28

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 68001546
Hyphenated Format 68001-546

Supplemental Identifiers

RxCUI
2601728
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 ANDA209085 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1000 mg/40mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (68001-546-41) / 40 mL in 1 VIAL
source: ndc

Packages (1)

68001-546-41 1 VIAL in 1 CARTON (68001-546-41) / 40 mL in 1 VIAL

Ingredients (1)

pemetrexed disodium (1000 mg/40mL)

Linked Drug Pages (1)

Pemetrexed ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "fa3ecbbb-86e3-6fca-e053-6394a90a56d9", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2601728"], "spl_set_id": ["61588f3c-4c06-4c35-a000-201dd1019093"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-546-41)  / 40 mL in 1 VIAL", "package_ndc": "68001-546-41", "marketing_start_date": "20230901"}], "brand_name": "Pemetrexed", "product_id": "68001-546_fa3ecbbb-86e3-6fca-e053-6394a90a56d9", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-546", "generic_name": "Pemetrexed disodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "1000 mg/40mL"}], "application_number": "ANDA209085", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}