Package 68083-171-01

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 68083-171-01
Digits Only 6808317101
Product NDC 68083-171
Product ID 68083-171_0d039035-85d1-40d4-8ee6-540026ab7a5c
Description

20 mL in 1 VIAL (68083-171-01)

Marketing

Marketing Status
Marketed Since 2017-05-29
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": "0d039035-85d1-40d4-8ee6-540026ab7a5c", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0368083171018", "0368083170011"], "unii": ["04ZR38536J"], "rxcui": ["1736784", "1736786"], "spl_set_id": ["d6178bc6-9dae-413f-8f47-de75d576c5b8"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL (68083-171-01)", "package_ndc": "68083-171-01", "marketing_start_date": "20170529"}], "brand_name": "Oxaliplatin", "product_id": "68083-171_0d039035-85d1-40d4-8ee6-540026ab7a5c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "68083-171", "generic_name": "Oxaliplatin", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "100 mg/20mL"}], "application_number": "ANDA207385", "marketing_category": "ANDA", "marketing_start_date": "20170529", "listing_expiration_date": "20261231"}