Package 68001-539-41

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 68001-539-41
Digits Only 6800153941
Product NDC 68001-539
Product ID 68001-539_eed98f1e-acdf-28da-e053-2a95a90a046c
Description

1 VIAL in 1 CARTON (68001-539-41) / 20 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-06-24
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": "eed98f1e-acdf-28da-e053-2a95a90a046c", "openfda": {"upc": ["0368001539418", "0368001538411"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["c9f34c00-1176-4f44-8cff-bae5bdc0c40f"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-539-41)  / 20 mL in 1 VIAL", "package_ndc": "68001-539-41", "marketing_start_date": "20220624"}], "brand_name": "Pemetrexed", "product_id": "68001-539_eed98f1e-acdf-28da-e053-2a95a90a046c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68001-539", "generic_name": "Pemetrexed disodium", "labeler_name": "BluePoint Laboratories", "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": "20220624", "listing_expiration_date": "20261231"}