Package 80425-0551-1

Brand: etodolac

Generic: etodolac
NDC Package

Package Facts

Identity

Package NDC 80425-0551-1
Digits Only 8042505511
Product NDC 80425-0551
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0551-1)

Marketing

Marketing Status
Marketed Since 2025-08-29
Brand etodolac
Generic etodolac
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d87cc75-7a10-46a2-e063-6294a90a6d49", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["197686"], "spl_set_id": ["3d865ff0-fc45-1e95-e063-6294a90a8e18"], "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": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0551-1)", "package_ndc": "80425-0551-1", "marketing_start_date": "20250829"}], "brand_name": "Etodolac", "product_id": "80425-0551_3d87cc75-7a10-46a2-e063-6294a90a6d49", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0551", "generic_name": "Etodolac", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etodolac", "active_ingredients": [{"name": "ETODOLAC", "strength": "400 mg/1"}], "application_number": "ANDA075074", "marketing_category": "ANDA", "marketing_start_date": "20250829", "listing_expiration_date": "20261231"}