Package 42367-531-33

Brand: pemfexy

Generic: pemetrexed
NDC Package

Package Facts

Identity

Package NDC 42367-531-33
Digits Only 4236753133
Product NDC 42367-531
Description

1 VIAL in 1 CARTON (42367-531-33) / 20 mL in 1 VIAL

Marketing

Marketing Status
Discontinued 2028-04-30
Brand pemfexy
Generic pemetrexed
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "efadeccf-c754-46aa-999e-4da07a4cd2ce", "openfda": {"unii": ["236Y2F7D9J"], "rxcui": ["2590672", "2590677"], "spl_set_id": ["2308f4e8-21c8-49c1-a5b8-deb8610bac6a"], "manufacturer_name": ["Eagle Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42367-531-33)  / 20 mL in 1 VIAL", "package_ndc": "42367-531-33", "marketing_end_date": "20280430", "marketing_start_date": "20220201"}], "brand_name": "Pemfexy", "product_id": "42367-531_efadeccf-c754-46aa-999e-4da07a4cd2ce", "dosage_form": "INJECTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "42367-531", "generic_name": "pemetrexed", "labeler_name": "Eagle Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemfexy", "active_ingredients": [{"name": "PEMETREXED MONOHYDRATE", "strength": "25 mg/mL"}], "application_number": "NDA209472", "marketing_category": "NDA", "marketing_end_date": "20280430", "marketing_start_date": "20220201"}