Package 50742-406-20

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 50742-406-20
Digits Only 5074240620
Product NDC 50742-406
Product ID 50742-406_a97dcd6a-aaa3-4b1b-b8d6-920945a0b788
Description

1 VIAL, SINGLE-USE in 1 CARTON (50742-406-20) / 20 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Discontinued 2026-03-31
Brand oxaliplatin
Generic oxaliplatin
Sample Package No

Linked Drug Pages (1)

Oxaliplatin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a97dcd6a-aaa3-4b1b-b8d6-920945a0b788", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0350742406203", "0350742405107"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["9613ae3d-72e2-40f7-8151-b43e915a6f1c"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50742-406-20)  / 20 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50742-406-20", "marketing_end_date": "20260331", "marketing_start_date": "20181029"}], "brand_name": "Oxaliplatin", "product_id": "50742-406_a97dcd6a-aaa3-4b1b-b8d6-920945a0b788", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "50742-406", "generic_name": "Oxaliplatin", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "100 mg/20mL"}], "application_number": "ANDA207562", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20181029"}