Package 71335-2565-1

Brand: linezolid

Generic: linezolid
NDC Package

Package Facts

Identity

Package NDC 71335-2565-1
Digits Only 7133525651
Product NDC 71335-2565
Product ID 71335-2565_c8913686-e7a0-451f-a345-9a8fd6e167df
Description

20 TABLET, FILM COATED in 1 BOTTLE (71335-2565-1)

Marketing

Marketing Status
Marketed Since 2025-01-28
Brand linezolid
Generic linezolid
Sample Package No

Linked Drug Pages (1)

Linezolid ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c8913686-e7a0-451f-a345-9a8fd6e167df", "openfda": {"nui": ["N0000175495", "M0361132"], "unii": ["ISQ9I6J12J"], "rxcui": ["311347"], "spl_set_id": ["ab1b4ab5-7338-4b01-963b-43eeb4c9cf1c"], "pharm_class_cs": ["Oxazolidinones [CS]"], "pharm_class_epc": ["Oxazolidinone Antibacterial [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2565-1)", "package_ndc": "71335-2565-1", "marketing_start_date": "20250128"}], "brand_name": "Linezolid", "product_id": "71335-2565_c8913686-e7a0-451f-a345-9a8fd6e167df", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Oxazolidinone Antibacterial [EPC]", "Oxazolidinones [CS]"], "product_ndc": "71335-2565", "generic_name": "Linezolid", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Linezolid", "active_ingredients": [{"name": "LINEZOLID", "strength": "600 mg/1"}], "application_number": "ANDA205517", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}