Package 55150-381-01

Brand: pemetrexed

Generic: pemetrexed
NDC Package

Package Facts

Identity

Package NDC 55150-381-01
Digits Only 5515038101
Product NDC 55150-381
Description

1 VIAL in 1 CARTON (55150-381-01) / 4 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-05-25
Brand pemetrexed
Generic pemetrexed
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d9465d8d-67cb-4650-8c84-a9293d45ac92", "openfda": {"upc": ["0355150382019", "0355150383016", "0355150381012"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077", "2601728"], "spl_set_id": ["737ead51-f73c-414f-b68f-d3affc27a225"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (55150-381-01)  / 4 mL in 1 VIAL", "package_ndc": "55150-381-01", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "55150-381_d9465d8d-67cb-4650-8c84-a9293d45ac92", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "55150-381", "generic_name": "Pemetrexed", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA214632", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}