Package 0409-2188-01
Brand: pemetrexed
Generic: pemetrexedPackage Facts
Identity
Package NDC
0409-2188-01
Digits Only
0409218801
Product NDC
0409-2188
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (0409-2188-01) / 20 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
pemetrexed
Generic
pemetrexed
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "54cf7e63-ef81-4ced-b833-a73ad8980230", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602363", "2602365", "2602366"], "spl_set_id": ["3ae68628-7ab0-4491-b3ae-6a8330b719c8"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-2188-01) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-2188-01", "marketing_start_date": "20220627"}], "brand_name": "PEMETREXED", "product_id": "0409-2188_54cf7e63-ef81-4ced-b833-a73ad8980230", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0409-2188", "generic_name": "PEMETREXED", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PEMETREXED", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "500 mg/20mL"}], "application_number": "NDA214218", "marketing_category": "NDA", "marketing_start_date": "20220627", "listing_expiration_date": "20261231"}