Package 0781-3518-76

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 0781-3518-76
Digits Only 0781351876
Product NDC 0781-3518
Product ID 0781-3518_764ab64b-c642-4314-83a9-efee79fe83a3
Description

1 VIAL in 1 CARTON (0781-3518-76) / 4 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-06-08
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": "764ab64b-c642-4314-83a9-efee79fe83a3", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602363", "2602365", "2602366"], "spl_set_id": ["7ac04ab7-7f8c-46ce-ab56-a7a08cd02ab3"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0781-3518-76)  / 4 mL in 1 VIAL", "package_ndc": "0781-3518-76", "marketing_start_date": "20220608"}], "brand_name": "Pemetrexed", "product_id": "0781-3518_764ab64b-c642-4314-83a9-efee79fe83a3", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0781-3518", "generic_name": "Pemetrexed disodium", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "100 mg/4mL"}], "application_number": "NDA214657", "marketing_category": "NDA", "marketing_start_date": "20220608", "listing_expiration_date": "20261231"}