oxaliplatin

Generic: oxaliplatin

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaliplatin
Generic Name oxaliplatin
Labeler ingenus pharmaceuticals, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

oxaliplatin 100 mg/20mL

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-406
Product ID 50742-406_a97dcd6a-aaa3-4b1b-b8d6-920945a0b788
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207562
Marketing Start 2018-10-29
Marketing End 2026-03-31

Pharmacologic Class

Established (EPC)
platinum-based drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742406
Hyphenated Format 50742-406

Supplemental Identifiers

RxCUI
1736776 1736781
UPC
0350742406203 0350742405107
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 ANDA207562 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/20mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 CARTON (50742-406-20) / 20 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

50742-406-20 1 VIAL, SINGLE-USE in 1 CARTON (50742-406-20) / 20 mL in 1 VIAL, SINGLE-USE

Ingredients (1)

oxaliplatin (100 mg/20mL)

Linked Drug Pages (1)

Oxaliplatin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "a97dcd6a-aaa3-4b1b-b8d6-920945a0b788", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0350742406203", "0350742405107"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["9613ae3d-72e2-40f7-8151-b43e915a6f1c"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50742-406-20)  / 20 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50742-406-20", "marketing_end_date": "20260331", "marketing_start_date": "20181029"}], "brand_name": "Oxaliplatin", "product_id": "50742-406_a97dcd6a-aaa3-4b1b-b8d6-920945a0b788", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "50742-406", "generic_name": "Oxaliplatin", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "100 mg/20mL"}], "application_number": "ANDA207562", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20181029"}