Package 0069-1542-20
Brand: doxorubicin hydrochloride
Generic: doxorubicin hydrochloridePackage Facts
Identity
Package NDC
0069-1542-20
Digits Only
0069154220
Product NDC
0069-1542
Description
1 VIAL, MULTI-DOSE in 1 CARTON (0069-1542-20) / 100 mL in 1 VIAL, MULTI-DOSE
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": "1e8e701d-b982-4671-b1ab-38b56826f23f", "openfda": {"unii": ["82F2G7BL4E"], "rxcui": ["1191138", "1790097", "1790099", "1790100"], "spl_set_id": ["1fd148fb-0fbc-4b6f-b790-23546fb46a71"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (0069-1542-20) / 100 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0069-1542-20", "marketing_start_date": "20240722"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "0069-1542_1e8e701d-b982-4671-b1ab-38b56826f23f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "0069-1542", "generic_name": "Doxorubicin Hydrochloride", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxorubicin Hydrochloride", "active_ingredients": [{"name": "DOXORUBICIN HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "NDA050629", "marketing_category": "NDA", "marketing_start_date": "20240722", "listing_expiration_date": "20261231"}