Package 70594-049-02

Brand: polymyxin b

Generic: polymyxin b sulfate
NDC Package

Package Facts

Identity

Package NDC 70594-049-02
Digits Only 7059404902
Product NDC 70594-049
Description

10 VIAL, GLASS in 1 CARTON (70594-049-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2018-10-01
Brand polymyxin b
Generic polymyxin b sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "OPHTHALMIC"], "spl_id": "fda91987-b6cd-4233-b09c-0f0300ad5df2", "openfda": {"upc": ["0370594049014"], "unii": ["19371312D4"], "rxcui": ["204509"], "spl_set_id": ["b56f18c0-ef5e-4ed9-a5af-f79f3cd189b6"], "manufacturer_name": ["Xellia Pharmaceuticals USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (70594-049-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS", "package_ndc": "70594-049-01", "marketing_start_date": "20181001"}, {"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (70594-049-02)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS", "package_ndc": "70594-049-02", "marketing_start_date": "20181001"}], "brand_name": "Polymyxin B", "product_id": "70594-049_fda91987-b6cd-4233-b09c-0f0300ad5df2", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "70594-049", "generic_name": "Polymyxin B Sulfate", "labeler_name": "Xellia Pharmaceuticals USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Polymyxin B", "active_ingredients": [{"name": "POLYMYXIN B SULFATE", "strength": "500000 [USP'U]/1"}], "application_number": "ANDA202766", "marketing_category": "ANDA", "marketing_start_date": "20181001", "listing_expiration_date": "20261231"}