Package 47335-049-40

Brand: doxorubicin hydrochloride

Generic: doxorubicin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47335-049-40
Digits Only 4733504940
Product NDC 47335-049
Description

1 VIAL, SINGLE-DOSE in 1 PACKAGE (47335-049-40) / 10 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2013-02-05
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": "dc7b9af1-bb7c-45f8-8f2e-d03c6e22898e", "openfda": {"upc": ["0347335050400"], "unii": ["82F2G7BL4E"], "rxcui": ["1790115", "1790127"], "spl_set_id": ["fbc48fa5-0bfb-4957-b13c-a56bb7a13b56"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 PACKAGE (47335-049-40)  / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "47335-049-40", "marketing_start_date": "20130205"}], "brand_name": "Doxorubicin Hydrochloride", "product_id": "47335-049_dc7b9af1-bb7c-45f8-8f2e-d03c6e22898e", "dosage_form": "INJECTABLE, LIPOSOMAL", "pharm_class": ["Anthracycline Topoisomerase Inhibitor [EPC]", "Anthracyclines [CS]", "Topoisomerase Inhibitors [MoA]"], "product_ndc": "47335-049", "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": "ANDA203263", "marketing_category": "ANDA", "marketing_start_date": "20130205", "listing_expiration_date": "20261231"}