Package 67184-0501-1

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 67184-0501-1
Digits Only 6718405011
Product NDC 67184-0501
Product ID 67184-0501_f9f54aa0-22e3-4958-b368-d89d716ac2fa
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (67184-0501-1) / 10 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2016-05-11
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": "f9f54aa0-22e3-4958-b368-d89d716ac2fa", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0367184050116", "0367184050215"], "unii": ["04ZR38536J"], "rxcui": ["1736784", "1736786"], "spl_set_id": ["e9e47f3c-9acc-44f5-b0bd-d26fe9d35d64"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67184-0501-1)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67184-0501-1", "marketing_start_date": "20160511"}], "brand_name": "Oxaliplatin", "product_id": "67184-0501_f9f54aa0-22e3-4958-b368-d89d716ac2fa", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "67184-0501", "generic_name": "Oxaliplatin", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "50 mg/10mL"}], "application_number": "ANDA204616", "marketing_category": "ANDA", "marketing_start_date": "20160511", "listing_expiration_date": "20261231"}