Package 75907-363-01

Brand: doxorubicin hydrochloride

Generic: doxorubicin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 75907-363-01
Digits Only 7590736301
Product NDC 75907-363
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (75907-363-01) / 10 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-06-27
Brand doxorubicin hydrochloride
Generic doxorubicin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0885dddf-727e-4692-92dd-a26c69cc278d", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1790115", "1790127"], "spl_set_id": ["0885dddf-727e-4692-92dd-a26c69cc278d"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (75907-363-01)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "75907-363-01", "marketing_start_date": "20250627"}], "brand_name": "doxorubicin hydrochloride", "product_id": "75907-363_0885dddf-727e-4692-92dd-a26c69cc278d", "dosage_form": "INJECTION, SUSPENSION, LIPOSOMAL", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "75907-363", "generic_name": "doxorubicin hydrochloride", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxorubicin hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA219199", "marketing_category": "ANDA", "marketing_start_date": "20250627", "listing_expiration_date": "20261231"}