oxaliplatin

Generic: oxaliplatin

Labeler: fosun pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxaliplatin
Generic Name oxaliplatin
Labeler fosun pharma usa inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

oxaliplatin 5 mg/mL

Manufacturer
FOSUN PHARMA USA INC.

Identifiers & Regulatory

Product NDC 72266-161
Product ID 72266-161_2b48f7c2-8c48-6b82-e063-6394a90a3baf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207325
Listing Expiration 2026-12-31
Marketing Start 2020-03-30

Pharmacologic Class

Established (EPC)
platinum-based drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266161
Hyphenated Format 72266-161

Supplemental Identifiers

RxCUI
1736776 1736781
UPC
0372266161017 0372266162014
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 ANDA207325 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 CARTON (72266-161-01) / 10 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

72266-161-01 1 VIAL, SINGLE-USE in 1 CARTON (72266-161-01) / 10 mL in 1 VIAL, SINGLE-USE

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": "2b48f7c2-8c48-6b82-e063-6394a90a3baf", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0372266161017", "0372266162014"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["fad0f147-6595-4412-87a7-2afca0192a96"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["FOSUN PHARMA USA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (72266-161-01)  / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "72266-161-01", "marketing_start_date": "20200330"}], "brand_name": "Oxaliplatin", "product_id": "72266-161_2b48f7c2-8c48-6b82-e063-6394a90a3baf", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "72266-161", "generic_name": "Oxaliplatin", "labeler_name": "FOSUN PHARMA USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA207325", "marketing_category": "ANDA", "marketing_start_date": "20200330", "listing_expiration_date": "20261231"}