Package 50742-340-01

Brand: Pemetrexed

Generic: Pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 50742-340-01
Digits Only 5074234001
Product NDC 50742-340
Product ID 50742-340_58f8fad9-d6df-4916-ad09-36416553173a
Description

1 VIAL in 1 CARTON (50742-340-01) / 4 mL in 1 VIAL

Marketing

Marketing Status
Discontinued 2026-02-28
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": "58f8fad9-d6df-4916-ad09-36416553173a", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["0346155f-a455-4044-8d5f-eacb97a8c8f0"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50742-340-01)  / 4 mL in 1 VIAL", "package_ndc": "50742-340-01", "marketing_end_date": "20260228", "marketing_start_date": "20220524"}], "brand_name": "Pemetrexed", "product_id": "50742-340_58f8fad9-d6df-4916-ad09-36416553173a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "50742-340", "generic_name": "Pemetrexed disodium", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA204890", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220524"}