pemetrexed

Generic: pemetrexed disodium

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pemetrexed disodium hemipentahydrate 500 mg/50mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-425
Product ID 72603-425_c754c764-7f07-480c-b130-c5ce64cf0b80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208696
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

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 72603425
Hyphenated Format 72603-425

Supplemental Identifiers

RxCUI
1728072 1728077
UPC
0372603425017 0372603325010
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 ANDA208696 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/50mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (72603-425-01) / 50 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

72603-425-01 1 VIAL, SINGLE-DOSE in 1 CARTON (72603-425-01) / 50 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

pemetrexed disodium hemipentahydrate (500 mg/50mL)

Linked Drug Pages (1)

Pemetrexed ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c754c764-7f07-480c-b130-c5ce64cf0b80", "openfda": {"upc": ["0372603425017", "0372603325010"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["64f4a9ed-26ff-4bc7-bef1-4faa98b35563"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72603-425-01)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72603-425-01", "marketing_start_date": "20241001"}], "brand_name": "Pemetrexed", "product_id": "72603-425_c754c764-7f07-480c-b130-c5ce64cf0b80", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "72603-425", "generic_name": "Pemetrexed disodium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "500 mg/50mL"}], "application_number": "ANDA208696", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}