Package 71288-146-50

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 71288-146-50
Digits Only 7128814650
Product NDC 71288-146
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-146-50) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-12-13
Brand pemetrexed
Generic pemetrexed disodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b369ac27-0118-4e53-be05-c9ba2dbf6875", "openfda": {"unii": ["9T47E4OM16"], "rxcui": ["1728072", "1728077", "2601728", "2602136"], "spl_set_id": ["b185f459-5489-4e18-8521-1686b5d16f67"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-146-50)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-146-50", "marketing_start_date": "20221213"}], "brand_name": "Pemetrexed", "product_id": "71288-146_b369ac27-0118-4e53-be05-c9ba2dbf6875", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "71288-146", "generic_name": "Pemetrexed disodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEPTAHYDRATE", "strength": "500 mg/20mL"}], "application_number": "ANDA215479", "marketing_category": "ANDA", "marketing_start_date": "20221213", "listing_expiration_date": "20261231"}