oxaliplatin
Generic: oxaliplatin
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
oxaliplatin
Generic Name
oxaliplatin
Labeler
northstar rx llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
oxaliplatin 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-420
Product ID
72603-420_9ebe158f-dd21-4bb8-ac13-d18162773cef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA217348
Listing Expiration
2027-12-31
Marketing Start
2024-01-11
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603420
Hyphenated Format
72603-420
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
ANDA217348 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (72603-420-01) / 10 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "9ebe158f-dd21-4bb8-ac13-d18162773cef", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0372603320015", "0372603420012"], "unii": ["04ZR38536J"], "rxcui": ["1736776", "1736781"], "spl_set_id": ["7dc8dfb1-dec8-43b3-b2ea-05eac054b2c6"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72603-420-01) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72603-420-01", "marketing_start_date": "20240111"}], "brand_name": "Oxaliplatin", "product_id": "72603-420_9ebe158f-dd21-4bb8-ac13-d18162773cef", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "72603-420", "generic_name": "Oxaliplatin", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaliplatin", "active_ingredients": [{"name": "OXALIPLATIN", "strength": "5 mg/mL"}], "application_number": "ANDA217348", "marketing_category": "ANDA", "marketing_start_date": "20240111", "listing_expiration_date": "20271231"}