cisplatin
Generic: cisplatin
Labeler: apotex corp.Drug Facts
Product Profile
Brand Name
cisplatin
Generic Name
cisplatin
Labeler
apotex corp.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
cisplatin 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
60505-6279
Product ID
60505-6279_0e147fbc-5660-4d80-b834-f069e8487f59
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218868
Listing Expiration
2026-12-31
Marketing Start
2024-09-13
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605056279
Hyphenated Format
60505-6279
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
cisplatin (source: ndc)
Generic Name
cisplatin (source: ndc)
Application Number
ANDA218868 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (60505-6279-0) / 50 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0e147fbc-5660-4d80-b834-f069e8487f59", "openfda": {"nui": ["N0000175413", "N0000175073"], "upc": ["0360505627905"], "unii": ["Q20Q21Q62J"], "rxcui": ["309311"], "spl_set_id": ["8d170f6f-37d7-41ce-aae2-33307a6ef3ae"], "pharm_class_epc": ["Platinum-based Drug [EPC]"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (60505-6279-0) / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "60505-6279-0", "marketing_start_date": "20240913"}], "brand_name": "CISplatin", "product_id": "60505-6279_0e147fbc-5660-4d80-b834-f069e8487f59", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Platinum-based Drug [EPC]", "Platinum-containing Compounds [EXT]"], "product_ndc": "60505-6279", "generic_name": "CISplatin", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CISplatin", "active_ingredients": [{"name": "CISPLATIN", "strength": "1 mg/mL"}], "application_number": "ANDA218868", "marketing_category": "ANDA", "marketing_start_date": "20240913", "listing_expiration_date": "20261231"}