Package 63323-450-50

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 63323-450-50
Digits Only 6332345050
Product NDC 63323-450
Product ID 63323-450_c7ff62a1-e697-4a7c-9907-59163f393528
Description

1 VIAL, SINGLE-USE in 1 CARTON (63323-450-50) / 20 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2022-05-25
Brand pemetrexed
Generic pemetrexed disodium
Sample Package No

Linked Drug Pages (1)

Pemetrexed ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c7ff62a1-e697-4a7c-9907-59163f393528", "openfda": {"upc": ["0363323450502", "0363323622008", "0363323621001", "0363323134105"], "unii": ["2PKU919BA9"], "rxcui": ["1728072", "1728077", "2601728", "2602136"], "spl_set_id": ["ae77f00f-d43b-4b75-afd5-a2a9cb7138da"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (63323-450-50)  / 20 mL in 1 VIAL, SINGLE-USE", "package_ndc": "63323-450-50", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "63323-450_c7ff62a1-e697-4a7c-9907-59163f393528", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "63323-450", "generic_name": "PEMETREXED DISODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "500 mg/20mL"}], "application_number": "ANDA090384", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}