Package 71288-172-21

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 71288-172-21
Digits Only 7128817221
Product NDC 71288-172
Product ID 71288-172_50b4c21f-714a-4a01-bf28-a856b19914d1
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (71288-172-21) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2024-01-11
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": "50b4c21f-714a-4a01-bf28-a856b19914d1", "openfda": {"nui": ["N0000175413", "N0000175073"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["ee2e0da9-5ae7-405b-8dd1-635be72bc439"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-172-21)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-172-21", "marketing_start_date": "20240111"}], "brand_name": "Oxaliplatin", "product_id": "71288-172_50b4c21f-714a-4a01-bf28-a856b19914d1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "71288-172", "generic_name": "Oxaliplatin", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA217348", "marketing_category": "ANDA", "marketing_start_date": "20240111", "listing_expiration_date": "20261231"}