irinotecan hydrochloride

Generic: irinotecan hydrochloride

Labeler: qilu pharmaceutical co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name irinotecan hydrochloride
Generic Name irinotecan hydrochloride
Labeler qilu pharmaceutical co., ltd.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

irinotecan hydrochloride 20 mg/mL

Manufacturer
Qilu Pharmaceutical Co., Ltd.

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
topoisomerase inhibitor [epc] topoisomerase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 671840513
Hyphenated Format 67184-0513

Supplemental Identifiers

RxCUI
1726319 1726324 1726333
UPC
0367184051311
UNII
042LAQ1IIS

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 irinotecan hydrochloride (source: ndc)
Generic Name irinotecan hydrochloride (source: ndc)
Application Number ANDA203380 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 CARTON (67184-0513-1) / 15 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

Ingredients (1)

irinotecan hydrochloride (20 mg/mL)

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"}