Package 70748-339-01
Brand: doxorubicin hydrochloride
Generic: doxorubicin hydrochloridePackage Facts
Identity
Package NDC
70748-339-01
Digits Only
7074833901
Product NDC
70748-339
Description
1 VIAL, SINGLE-USE in 1 CARTON (70748-339-01) / 10 mL in 1 VIAL, SINGLE-USE
Marketing
Marketing Status
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": "e9f76142-15d0-4234-8f2e-5f5014160eff", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1790115", "1790127"], "spl_set_id": ["0f8eb9a1-74d0-47fd-94b8-a65b29006521"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (70748-339-01) / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "70748-339-01", "marketing_start_date": "20240826"}], "brand_name": "DOXORUBICIN HYDROCHLORIDE", "product_id": "70748-339_e9f76142-15d0-4234-8f2e-5f5014160eff", "dosage_form": "INJECTION, SUSPENSION, LIPOSOMAL", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "70748-339", "generic_name": "DOXORUBICIN HYDROCHLORIDE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXORUBICIN HYDROCHLORIDE", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA215178", "marketing_category": "ANDA", "marketing_start_date": "20240826", "listing_expiration_date": "20261231"}