Package 67184-0504-1

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 67184-0504-1
Digits Only 6718405041
Product NDC 67184-0504
Product ID 67184-0504_0dc735ab-c4c9-4e19-bb80-8a439be7208c
Description

1 VIAL in 1 CARTON (67184-0504-1) / 20 mL in 1 VIAL

Marketing

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

Linked Drug Pages (1)

Pemetrexed ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0dc735ab-c4c9-4e19-bb80-8a439be7208c", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["46a9b89d-7135-4e0c-b8e4-52580554769b"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67184-0504-1)  / 20 mL in 1 VIAL", "package_ndc": "67184-0504-1", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "67184-0504_0dc735ab-c4c9-4e19-bb80-8a439be7208c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "67184-0504", "generic_name": "Pemetrexed disodium", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "500 mg/20mL"}], "application_number": "ANDA204890", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}