Package 68001-468-36

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 68001-468-36
Digits Only 6800146836
Product NDC 68001-468
Description

1 VIAL in 1 CARTON (68001-468-36) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2020-12-09
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": "2ee49254-54a3-0865-e063-6294a90a2974", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["b6083405-9b45-4d2c-e053-2995a90ad9ef"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68001-468-36)  / 10 mL in 1 VIAL", "package_ndc": "68001-468-36", "marketing_start_date": "20201209"}, {"sample": false, "description": "1 VIAL in 1 CARTON (68001-468-37)  / 20 mL in 1 VIAL", "package_ndc": "68001-468-37", "marketing_start_date": "20201209"}], "brand_name": "Oxaliplatin", "product_id": "68001-468_2ee49254-54a3-0865-e063-6294a90a2974", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "68001-468", "generic_name": "Oxaliplatin", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA204368", "marketing_category": "ANDA", "marketing_start_date": "20201209", "listing_expiration_date": "20261231"}