Package 68001-544-41

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 68001-544-41
Digits Only 6800154441
Product NDC 68001-544
Product ID 68001-544_0759eb55-d7ae-c87a-e063-6394a90abe08
Description

1 VIAL in 1 CARTON (68001-544-41) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-09-01
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": "0759eb55-d7ae-c87a-e063-6394a90abe08", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["4cc1574b-3d2f-489b-9ad3-55695bb97200"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-544-41)  / 20 mL in 1 VIAL", "package_ndc": "68001-544-41", "marketing_start_date": "20220901"}], "brand_name": "Pemetrexed", "product_id": "68001-544_0759eb55-d7ae-c87a-e063-6394a90abe08", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-544", "generic_name": "Pemetrexed disodium", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "500 mg/20mL"}], "application_number": "ANDA203774", "marketing_category": "ANDA", "marketing_start_date": "20220901", "listing_expiration_date": "20261231"}