Package 25021-261-50
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
25021-261-50
Digits Only
2502126150
Product NDC
25021-261
Description
1 VIAL in 1 CARTON (25021-261-50) / 20 mL in 1 VIAL
Marketing
Marketing Status
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": "f9386c39-eee1-4407-91b7-f55bc710897a", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["fa8f1f52-3f05-4ae8-bfec-7f0a029e6825"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-261-50) / 20 mL in 1 VIAL", "package_ndc": "25021-261-50", "marketing_start_date": "20241215"}], "brand_name": "Pemetrexed", "product_id": "25021-261_f9386c39-eee1-4407-91b7-f55bc710897a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "25021-261", "generic_name": "Pemetrexed Disodium", "labeler_name": "Sagent Pharmaceuticals", "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": "20241215", "listing_expiration_date": "20261231"}