Package 60505-6068-0
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
60505-6068-0
Digits Only
6050560680
Product NDC
60505-6068
Description
1 VIAL in 1 CARTON (60505-6068-0) / 30 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": "bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602136"], "spl_set_id": ["2e86f231-e0c7-2d43-2920-6c42d2469d11"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (60505-6068-0) / 30 mL in 1 VIAL", "package_ndc": "60505-6068-0", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "60505-6068_bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "60505-6068", "generic_name": "Pemetrexed disodium", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "750 mg/30mL"}], "application_number": "ANDA209851", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}