Package 55150-128-24

Brand: oxacillin

Generic: oxacillin sodium
NDC Package

Package Facts

Identity

Package NDC 55150-128-24
Digits Only 5515012824
Product NDC 55150-128
Description

10 VIAL in 1 BOX (55150-128-24) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2013-01-18
Brand oxacillin
Generic oxacillin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0570fa17-5fe7-4647-9dde-d6097388a4e8", "openfda": {"upc": ["0355150128242", "0355150127153"], "unii": ["G0V6C994Q5"], "rxcui": ["1743547", "1743549"], "spl_set_id": ["81e90279-9889-47bd-974b-334c181f295c"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 BOX (55150-128-24)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "55150-128-24", "marketing_start_date": "20130118"}], "brand_name": "Oxacillin", "product_id": "55150-128_0570fa17-5fe7-4647-9dde-d6097388a4e8", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "55150-128", "generic_name": "Oxacillin Sodium", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxacillin", "active_ingredients": [{"name": "OXACILLIN SODIUM", "strength": "2 g/1"}], "application_number": "ANDA201539", "marketing_category": "ANDA", "marketing_start_date": "20130118", "listing_expiration_date": "20261231"}