oxaliplatin

Generic: oxaliplatin

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaliplatin
Generic Name oxaliplatin
Labeler bluepoint laboratories
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

oxaliplatin 5 mg/mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-468
Product ID 68001-468_2ee49254-54a3-0865-e063-6294a90a2974
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204368
Listing Expiration 2026-12-31
Marketing Start 2020-12-09

Pharmacologic Class

Established (EPC)
platinum-based drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001468
Hyphenated Format 68001-468

Supplemental Identifiers

RxCUI
1736776 1736781
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 ANDA204368 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (68001-468-36) / 10 mL in 1 VIAL
  • 1 VIAL in 1 CARTON (68001-468-37) / 20 mL in 1 VIAL
source: ndc

Packages (2)

68001-468-36 1 VIAL in 1 CARTON (68001-468-36) / 10 mL in 1 VIAL 68001-468-37 1 VIAL in 1 CARTON (68001-468-37) / 20 mL in 1 VIAL

Ingredients (1)

oxaliplatin (5 mg/mL)

Linked Drug Pages (1)

Oxaliplatin ndc-match (0.9)

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"}