doxorubicin hydrochloride

Generic: doxorubicin hydrochloride

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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
INTRAVENOUS
Active Ingredients

doxorubicin hydrochloride 2 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

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
anthracycline topoisomerase inhibitor [epc] anthracyclines [cs] topoisomerase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439093
Hyphenated Format 0143-9093

Supplemental Identifiers

RxCUI
1790095 1790103
UNII
82F2G7BL4E

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 doxorubicin hydrochloride (source: ndc)
Generic Name doxorubicin hydrochloride (source: ndc)
Application Number ANDA062921 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX (0143-9093-01) / 25 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

doxorubicin hydrochloride (2 mg/mL)

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"}