Package 68001-546-41

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 68001-546-41
Digits Only 6800154641
Product NDC 68001-546
Product ID 68001-546_fa3ecbbb-86e3-6fca-e053-6394a90a56d9
Description

1 VIAL in 1 CARTON (68001-546-41) / 40 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-09-01
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": "fa3ecbbb-86e3-6fca-e053-6394a90a56d9", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2601728"], "spl_set_id": ["61588f3c-4c06-4c35-a000-201dd1019093"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-546-41)  / 40 mL in 1 VIAL", "package_ndc": "68001-546-41", "marketing_start_date": "20230901"}], "brand_name": "Pemetrexed", "product_id": "68001-546_fa3ecbbb-86e3-6fca-e053-6394a90a56d9", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-546", "generic_name": "Pemetrexed disodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "1000 mg/40mL"}], "application_number": "ANDA209085", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}