Package 0703-3985-01

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 0703-3985-01
Digits Only 0703398501
Product NDC 0703-3985
Product ID 0703-3985_b349bdd1-79de-44e6-ab0b-892a65bda6f6
Description

1 VIAL, SINGLE-USE in 1 CARTON (0703-3985-01) / 10 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": "b349bdd1-79de-44e6-ab0b-892a65bda6f6", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0307033986012", "0307033985015"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["9e51cc79-620c-48d7-b267-78e43c1ef6e4"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0703-3985-01)  / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0703-3985-01", "marketing_end_date": "20260331", "marketing_start_date": "20090811"}], "brand_name": "Oxaliplatin", "product_id": "0703-3985_b349bdd1-79de-44e6-ab0b-892a65bda6f6", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "0703-3985", "generic_name": "Oxaliplatin", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "50 mg/10mL"}], "application_number": "NDA022160", "marketing_category": "NDA", "marketing_end_date": "20260331", "marketing_start_date": "20090811"}