Package 63759-3048-1

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 63759-3048-1
Digits Only 6375930481
Product NDC 63759-3048
Description

1 VIAL in 1 CARTON (63759-3048-1) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-01-01
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": "b0e3847a-fdcf-405c-823c-180fa8dad9c2", "openfda": {"upc": ["0363759304912", "0363759304813", "0363759305018"], "unii": ["F4GSH45R4C"], "rxcui": ["2637958", "2637966", "2637968"], "spl_set_id": ["fe432994-e61b-4a87-8c98-cc20b847d0fe"], "manufacturer_name": ["Shilpa Medicare Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63759-3048-1)  / 10 mL in 1 VIAL", "package_ndc": "63759-3048-1", "marketing_start_date": "20240101"}], "brand_name": "Pemetrexed", "product_id": "63759-3048_b0e3847a-fdcf-405c-823c-180fa8dad9c2", "dosage_form": "INJECTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "63759-3048", "generic_name": "Pemetrexed disodium", "labeler_name": "Shilpa Medicare Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/10mL"}], "application_number": "NDA215179", "marketing_category": "NDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}