irinotecan hydrochloride
Generic: irinotecan hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
irinotecan hydrochloride
Generic Name
irinotecan hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
irinotecan hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9702
Product ID
0143-9702_204eb37a-642f-4321-9466-414c32a6bbce
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091032
Listing Expiration
2026-12-31
Marketing Start
2010-12-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439702
Hyphenated Format
0143-9702
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
ANDA091032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 2 mL in 1 VIAL, GLASS (0143-9702-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "204eb37a-642f-4321-9466-414c32a6bbce", "openfda": {"upc": ["0301439701019"], "unii": ["042LAQ1IIS"], "rxcui": ["1726319", "1726324"], "spl_set_id": ["be716692-6b4f-47b6-83d1-01665861626b"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, GLASS (0143-9702-01)", "package_ndc": "0143-9702-01", "marketing_start_date": "20101220"}], "brand_name": "Irinotecan Hydrochloride", "product_id": "0143-9702_204eb37a-642f-4321-9466-414c32a6bbce", "dosage_form": "INJECTION", "pharm_class": ["Topoisomerase Inhibitor [EPC]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9702", "generic_name": "Irinotecan Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Irinotecan Hydrochloride", "active_ingredients": [{"name": "IRINOTECAN HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA091032", "marketing_category": "ANDA", "marketing_start_date": "20101220", "listing_expiration_date": "20261231"}