Package 70954-785-10

Brand: nabumetone

Generic: nabumetone
NDC Package

Package Facts

Identity

Package NDC 70954-785-10
Digits Only 7095478510
Product NDC 70954-785
Description

100 TABLET, FILM COATED in 1 BOTTLE (70954-785-10)

Marketing

Marketing Status
Marketed Since 2025-01-07
Brand nabumetone
Generic nabumetone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e87289f4-d4f9-4510-aaa5-51f8f8167658", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0370954785101", "0370954784104", "0370954784203", "0370954785200"], "unii": ["LW0TIW155Z"], "rxcui": ["311892", "311893"], "spl_set_id": ["e87289f4-d4f9-4510-aaa5-51f8f8167658"], "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": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70954-785-10)", "package_ndc": "70954-785-10", "marketing_start_date": "20250107"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70954-785-20)", "package_ndc": "70954-785-20", "marketing_start_date": "20250107"}], "brand_name": "Nabumetone", "product_id": "70954-785_e87289f4-d4f9-4510-aaa5-51f8f8167658", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70954-785", "generic_name": "Nabumetone", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "750 mg/1"}], "application_number": "ANDA219118", "marketing_category": "ANDA", "marketing_start_date": "20250107", "listing_expiration_date": "20261231"}