Package 67184-0510-1

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 67184-0510-1
Digits Only 6718405101
Product NDC 67184-0510
Product ID 67184-0510_e78605b3-b28b-4634-9a58-d4bda67832ba
Description

1 VIAL, SINGLE-USE in 1 CARTON (67184-0510-1) / 40 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2016-06-07
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": "e78605b3-b28b-4634-9a58-d4bda67832ba", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0367184050918", "0367184051014", "0367184050819"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781", "1797528"], "spl_set_id": ["33d4f4b4-bb4e-46af-9e89-df20154436d0"], "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-USE in 1 CARTON (67184-0510-1)  / 40 mL in 1 VIAL, SINGLE-USE", "package_ndc": "67184-0510-1", "marketing_start_date": "20160607"}], "brand_name": "Oxaliplatin", "product_id": "67184-0510_e78605b3-b28b-4634-9a58-d4bda67832ba", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "67184-0510", "generic_name": "Oxaliplatin", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "200 mg/40mL"}], "application_number": "ANDA204368", "marketing_category": "ANDA", "marketing_start_date": "20160607", "listing_expiration_date": "20261231"}