Package 0009-5138-02

Brand: zyvox

Generic: linezolid
NDC Package

Package Facts

Identity

Package NDC 0009-5138-02
Digits Only 0009513802
Product NDC 0009-5138
Product ID 0009-5138_c038c5e0-0b25-4a00-82d9-b7ff930fe948
Description

20 TABLET, FILM COATED in 1 BOTTLE (0009-5138-02)

Marketing

Marketing Status
Discontinued 2027-02-28
Brand zyvox
Generic linezolid
Sample Package No

Linked Drug Pages (1)

Zyvox ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c038c5e0-0b25-4a00-82d9-b7ff930fe948", "openfda": {"nui": ["N0000175495", "M0361132"], "upc": ["0300095138023"], "unii": ["ISQ9I6J12J"], "rxcui": ["262091", "311345", "311347", "581614", "1662278", "1662280", "1662285", "1662286"], "spl_set_id": ["6e70e63b-bfd5-478d-a8ee-8ba22c9efabd"], "pharm_class_cs": ["Oxazolidinones [CS]"], "pharm_class_epc": ["Oxazolidinone Antibacterial [EPC]"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (0009-5138-02)", "package_ndc": "0009-5138-02", "marketing_end_date": "20270228", "marketing_start_date": "20151012"}], "brand_name": "Zyvox", "product_id": "0009-5138_c038c5e0-0b25-4a00-82d9-b7ff930fe948", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Oxazolidinone Antibacterial [EPC]", "Oxazolidinones [CS]"], "product_ndc": "0009-5138", "generic_name": "linezolid", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zyvox", "active_ingredients": [{"name": "LINEZOLID", "strength": "600 mg/1"}], "application_number": "NDA021130", "marketing_category": "NDA", "marketing_end_date": "20270228", "marketing_start_date": "20151012"}