doxorubicin hydrochloride

Generic: doxorubicin hydrochloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxorubicin hydrochloride
Generic Name doxorubicin hydrochloride
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

doxorubicin hydrochloride 2 mg/mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-827
Product ID 62756-827_d95f19dc-a686-42c7-88dc-997659b803df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091418
Listing Expiration 2026-12-31
Marketing Start 2012-02-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756827
Hyphenated Format 62756-827

Supplemental Identifiers

RxCUI
1191138 1790100
UPC
0362756827400 0362756826403
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 ANDA091418 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) / 100 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

62756-827-40 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) / 100 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

doxorubicin hydrochloride (2 mg/mL)

Linked Drug Pages (1)

DOXOrubicin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "d95f19dc-a686-42c7-88dc-997659b803df", "openfda": {"upc": ["0362756827400", "0362756826403"], "unii": ["82F2G7BL4E"], "rxcui": ["1191138", "1790100"], "spl_set_id": ["6bcde92b-e584-4919-866a-68847ea201ba"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40)  / 100 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "62756-827-40", "marketing_start_date": "20120220"}], "brand_name": "DOXOrubicin Hydrochloride", "product_id": "62756-827_d95f19dc-a686-42c7-88dc-997659b803df", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "62756-827", "generic_name": "DOXOrubicin Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXOrubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA091418", "marketing_category": "ANDA", "marketing_start_date": "20120220", "listing_expiration_date": "20261231"}