Package 31722-358-20

Brand: oxaliplatin

Generic: oxaliplatin
NDC Package

Package Facts

Identity

Package NDC 31722-358-20
Digits Only 3172235820
Product NDC 31722-358
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (31722-358-20) / 20 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-01-27
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": "3fee20f4-5fee-8b4e-e063-6294a90a1a0a", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0331722357104", "0331722358200"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["b0799e39-7b1e-430a-b159-062b39521001"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (31722-358-20)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "31722-358-20", "marketing_start_date": "20250127"}], "brand_name": "Oxaliplatin", "product_id": "31722-358_3fee20f4-5fee-8b4e-e063-6294a90a1a0a", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "31722-358", "generic_name": "Oxaliplatin", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "100 mg/20mL"}], "application_number": "ANDA217925", "marketing_category": "ANDA", "marketing_start_date": "20250127", "listing_expiration_date": "20261231"}