Package 61703-363-22

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 61703-363-22
Digits Only 6170336322
Product NDC 61703-363
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-22) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2009-08-10
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": "ecdfccf3-58e8-47ce-89d3-53a4d3e3af21", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["e51a62ba-d163-4c57-835c-8c86cf097e40"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-18)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "61703-363-18", "marketing_start_date": "20090810"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (61703-363-22)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "61703-363-22", "marketing_start_date": "20090810"}], "brand_name": "Oxaliplatin", "product_id": "61703-363_ecdfccf3-58e8-47ce-89d3-53a4d3e3af21", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "61703-363", "generic_name": "OXALIPLATIN", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA078813", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20261231"}