Package 71335-0393-7

Brand: oxaprozin

Generic: oxaprozin
NDC Package

Package Facts

Identity

Package NDC 71335-0393-7
Digits Only 7133503937
Product NDC 71335-0393
Description

120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)

Marketing

Marketing Status
Marketed Since 2007-09-12
Brand oxaprozin
Generic oxaprozin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "115ad76f-3895-41b7-bc5a-a7a0975aca9d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["MHJ80W9LRB"], "rxcui": ["312132"], "spl_set_id": ["dcb85e40-3427-4e56-910d-c1b07bb5c0fa"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0393-1)", "package_ndc": "71335-0393-1", "marketing_start_date": "20070912"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-0393-2)", "package_ndc": "71335-0393-2", "marketing_start_date": "20070912"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-0393-3)", "package_ndc": "71335-0393-3", "marketing_start_date": "20070912"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0393-4)", "package_ndc": "71335-0393-4", "marketing_start_date": "20070912"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0393-5)", "package_ndc": "71335-0393-5", "marketing_start_date": "20070912"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-0393-6)", "package_ndc": "71335-0393-6", "marketing_start_date": "20070912"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0393-7)", "package_ndc": "71335-0393-7", "marketing_start_date": "20070912"}], "brand_name": "Oxaprozin", "product_id": "71335-0393_115ad76f-3895-41b7-bc5a-a7a0975aca9d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-0393", "generic_name": "Oxaprozin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxaprozin", "active_ingredients": [{"name": "OXAPROZIN", "strength": "600 mg/1"}], "application_number": "ANDA075855", "marketing_category": "ANDA", "marketing_start_date": "20010131", "listing_expiration_date": "20261231"}