oxaliplatin

Generic: oxaliplatin

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaliplatin
Generic Name oxaliplatin
Labeler camber pharmaceuticals, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

oxaliplatin 50 mg/10mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-357
Product ID 31722-357_3fee20f4-5fee-8b4e-e063-6294a90a1a0a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217925
Listing Expiration 2026-12-31
Marketing Start 2025-01-27

Pharmacologic Class

Established (EPC)
platinum-based drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722357
Hyphenated Format 31722-357

Supplemental Identifiers

RxCUI
1736776 1736781
UPC
0331722357104 0331722358200
UNII
04ZR38536J
NUI
N0000175413 N0000175073

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name oxaliplatin (source: ndc)
Generic Name oxaliplatin (source: ndc)
Application Number ANDA217925 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/10mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (31722-357-10) / 10 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

31722-357-10 1 VIAL, SINGLE-DOSE in 1 CARTON (31722-357-10) / 10 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

oxaliplatin (50 mg/10mL)

Linked Drug Pages (1)

Oxaliplatin ndc-match (0.9)

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 (31722-357-10)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "31722-357-10", "marketing_start_date": "20250127"}], "brand_name": "Oxaliplatin", "product_id": "31722-357_3fee20f4-5fee-8b4e-e063-6294a90a1a0a", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "31722-357", "generic_name": "Oxaliplatin", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "50 mg/10mL"}], "application_number": "ANDA217925", "marketing_category": "ANDA", "marketing_start_date": "20250127", "listing_expiration_date": "20261231"}