Package 72603-425-01
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
72603-425-01
Digits Only
7260342501
Product NDC
72603-425
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (72603-425-01) / 50 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
pemetrexed
Generic
pemetrexed disodium
Sample Package
No
Linked Drug Pages (1)
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"}