doxorubicin hydrochloride
Generic: doxorubicin hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
doxorubicin hydrochloride
Generic Name
doxorubicin hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
doxorubicin hydrochloride 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9093
Product ID
0143-9093_3b0d5f19-5eab-4729-8fbf-3b988cbc6d04
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062921
Listing Expiration
2026-12-31
Marketing Start
2018-01-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439093
Hyphenated Format
0143-9093
Supplemental Identifiers
RxCUI
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
doxorubicin hydrochloride (source: ndc)
Generic Name
doxorubicin hydrochloride (source: ndc)
Application Number
ANDA062921 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 1 VIAL in 1 BOX (0143-9093-01) / 25 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3b0d5f19-5eab-4729-8fbf-3b988cbc6d04", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1790095", "1790103"], "spl_set_id": ["f62aa88d-1e25-4049-87ec-99d42edd1d31"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9093-01) / 25 mL in 1 VIAL", "package_ndc": "0143-9093-01", "marketing_start_date": "20180119"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "0143-9093_3b0d5f19-5eab-4729-8fbf-3b988cbc6d04", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0143-9093", "generic_name": "Doxorubicin Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxorubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA062921", "marketing_category": "ANDA", "marketing_start_date": "20180119", "listing_expiration_date": "20261231"}