Package 0781-3317-80

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 0781-3317-80
Digits Only 0781331780
Product NDC 0781-3317
Product ID 0781-3317_f3766495-fce3-461c-8c95-e890f5e3383f
Description

1 VIAL, SINGLE-USE in 1 CARTON (0781-3317-80) / 20 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2015-03-01
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": "f3766495-fce3-461c-8c95-e890f5e3383f", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["ab162009-6f84-4d56-ab56-5e84409ec814"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0781-3317-80)  / 20 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0781-3317-80", "marketing_start_date": "20150301"}], "brand_name": "Oxaliplatin", "product_id": "0781-3317_f3766495-fce3-461c-8c95-e890f5e3383f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "0781-3317", "generic_name": "Oxaliplatin", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA078817", "marketing_category": "ANDA", "marketing_start_date": "20150301", "listing_expiration_date": "20261231"}