Package 68001-535-41

Brand: pemetrexed

Generic: pemetrexed
NDC Package

Package Facts

Identity

Package NDC 68001-535-41
Digits Only 6800153541
Product NDC 68001-535
Description

1 VIAL in 1 CARTON (68001-535-41) / 4 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-07-04
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": "044d8cd9-3d5c-5c5e-e063-6394a90a3bbf", "openfda": {"upc": ["0368001537414", "0368001535410"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077", "2601728"], "spl_set_id": ["495c6751-8d6f-4093-8108-9bed283fce03"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-535-41)  / 4 mL in 1 VIAL", "package_ndc": "68001-535-41", "marketing_start_date": "20220704"}], "brand_name": "Pemetrexed", "product_id": "68001-535_044d8cd9-3d5c-5c5e-e063-6394a90a3bbf", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-535", "generic_name": "Pemetrexed", "labeler_name": "BluePoint Laboratories", "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": "20220704", "listing_expiration_date": "20261231"}