irinotecan hydrochloride
Generic: irinotecan hydrochloride
Labeler: qilu pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
irinotecan hydrochloride
Generic Name
irinotecan hydrochloride
Labeler
qilu pharmaceutical co., ltd.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
irinotecan hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67184-0513
Product ID
67184-0513_5faaf9ca-ed20-4ebf-9e7f-1d3a0ca60056
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203380
Listing Expiration
2026-12-31
Marketing Start
2016-05-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
671840513
Hyphenated Format
67184-0513
Supplemental Identifiers
RxCUI
UPC
UNII
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
irinotecan hydrochloride (source: ndc)
Generic Name
irinotecan hydrochloride (source: ndc)
Application Number
ANDA203380 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL, SINGLE-USE in 1 CARTON (67184-0513-1) / 15 mL in 1 VIAL, SINGLE-USE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "5faaf9ca-ed20-4ebf-9e7f-1d3a0ca60056", "openfda": {"upc": ["0367184051311"], "unii": ["042LAQ1IIS"], "rxcui": ["1726319", "1726324", "1726333"], "spl_set_id": ["afcdde49-ec0c-4c56-a1af-2917185b1a08"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (67184-0513-1) / 15 mL in 1 VIAL, SINGLE-USE", "package_ndc": "67184-0513-1", "marketing_start_date": "20160503"}], "brand_name": "Irinotecan Hydrochloride", "product_id": "67184-0513_5faaf9ca-ed20-4ebf-9e7f-1d3a0ca60056", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Topoisomerase Inhibitor [EPC]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "67184-0513", "generic_name": "Irinotecan Hydrochloride", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irinotecan Hydrochloride", "active_ingredients": [{"name": "IRINOTECAN HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA203380", "marketing_category": "ANDA", "marketing_start_date": "20160503", "listing_expiration_date": "20261231"}