Package 68083-314-01

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 68083-314-01
Digits Only 6808331401
Product NDC 68083-314
Description

1 VIAL, SINGLE-USE in 1 CARTON (68083-314-01) / 40 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2017-11-06
Brand oxaliplatin
Generic oxaliplatin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "4ccc9b7c-9bf8-4e27-8c38-f98e80360fcf", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0368083314019", "0368083176013", "0368083177010"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781", "1797528"], "spl_set_id": ["a6f89dc3-a594-4b5b-8728-272e20c1ecb5"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (68083-314-01)  / 40 mL in 1 VIAL, SINGLE-USE", "package_ndc": "68083-314-01", "marketing_start_date": "20171106"}], "brand_name": "Oxaliplatin", "product_id": "68083-314_4ccc9b7c-9bf8-4e27-8c38-f98e80360fcf", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "68083-314", "generic_name": "Oxaliplatin", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA207325", "marketing_category": "ANDA", "marketing_start_date": "20171106", "listing_expiration_date": "20261231"}