Package 72603-101-01

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 72603-101-01
Digits Only 7260310101
Product NDC 72603-101
Product ID 72603-101_f7b91231-4045-45a6-97c3-72fa9deaccf6
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72603-101-01) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Discontinued 2027-03-31
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": "f7b91231-4045-45a6-97c3-72fa9deaccf6", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0372603101010", "0372603301014"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["f299b2d2-86ed-4fb8-822e-65455a0bb75a"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72603-101-01)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72603-101-01", "marketing_end_date": "20270331", "marketing_start_date": "20190617"}], "brand_name": "Oxaliplatin", "product_id": "72603-101_f7b91231-4045-45a6-97c3-72fa9deaccf6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "72603-101", "generic_name": "Oxaliplatin", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA207325", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20190617"}