Package 68788-7597-3

Brand: nabumetone

Generic: nabumetone
NDC Package

Package Facts

Identity

Package NDC 68788-7597-3
Digits Only 6878875973
Product NDC 68788-7597
Description

30 TABLET in 1 BOTTLE (68788-7597-3)

Marketing

Marketing Status
Marketed Since 2020-02-13
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": "1f953669-46a2-42c0-999e-60f78dc641c8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["LW0TIW155Z"], "rxcui": ["311893"], "spl_set_id": ["455c9992-39a0-4353-a121-57e700c77942"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7597-1)", "package_ndc": "68788-7597-1", "marketing_start_date": "20200213"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7597-2)", "package_ndc": "68788-7597-2", "marketing_start_date": "20200213"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7597-3)", "package_ndc": "68788-7597-3", "marketing_start_date": "20200213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7597-6)", "package_ndc": "68788-7597-6", "marketing_start_date": "20200213"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68788-7597-8)", "package_ndc": "68788-7597-8", "marketing_start_date": "20200213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7597-9)", "package_ndc": "68788-7597-9", "marketing_start_date": "20200213"}], "brand_name": "Nabumetone", "product_id": "68788-7597_1f953669-46a2-42c0-999e-60f78dc641c8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7597", "generic_name": "Nabumetone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nabumetone", "active_ingredients": [{"name": "NABUMETONE", "strength": "750 mg/1"}], "application_number": "ANDA078420", "marketing_category": "ANDA", "marketing_start_date": "20200213", "listing_expiration_date": "20261231"}