Package 83831-111-01

Brand: pemetrexed dipotassium

Generic: pemetrexed dipotassium
NDC Package

Package Facts

Identity

Package NDC 83831-111-01
Digits Only 8383111101
Product NDC 83831-111
Product ID 83831-111_0c1baa15-83bb-45a0-a3ab-855a4fee9129
Description

1 VIAL in 1 CARTON (83831-111-01) / 4 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-01-01
Brand pemetrexed dipotassium
Generic pemetrexed dipotassium
Sample Package No

Linked Drug Pages (1)

PEMETREXED DIPOTASSIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0c1baa15-83bb-45a0-a3ab-855a4fee9129", "openfda": {"nui": ["N0000175584", "N0000000111"], "upc": ["0383831111016", "0383831112013"], "unii": ["04Q9AIZ7NO"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["adc9ce4c-926a-4ee8-bd0d-d06fc89c17fc"], "pharm_class_epc": ["Folate Analog Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Folic Acid Metabolism Inhibitors [MoA]"], "manufacturer_name": ["Avyxa Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (83831-111-01)  / 4 mL in 1 VIAL", "package_ndc": "83831-111-01", "marketing_start_date": "20250101"}], "brand_name": "PEMETREXED DIPOTASSIUM", "product_id": "83831-111_0c1baa15-83bb-45a0-a3ab-855a4fee9129", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "83831-111", "generic_name": "pemetrexed dipotassium", "labeler_name": "Avyxa Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PEMETREXED DIPOTASSIUM", "active_ingredients": [{"name": "PEMETREXED", "strength": "100 mg/4mL"}], "application_number": "NDA210661", "marketing_category": "NDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}