Package 68788-8673-3

Brand: etodolac

Generic: etodolac
NDC Package

Package Facts

Identity

Package NDC 68788-8673-3
Digits Only 6878886733
Product NDC 68788-8673
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-8673-3)

Marketing

Marketing Status
Marketed Since 2024-05-22
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": "fe4239d0-8003-4b3e-9770-01b21a0dd1d8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["197686"], "spl_set_id": ["117b3005-a8ec-4f76-824c-95ec42dc87a1"], "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, FILM COATED in 1 BOTTLE (68788-8673-1)", "package_ndc": "68788-8673-1", "marketing_start_date": "20240522"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8673-2)", "package_ndc": "68788-8673-2", "marketing_start_date": "20240522"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8673-3)", "package_ndc": "68788-8673-3", "marketing_start_date": "20240522"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8673-6)", "package_ndc": "68788-8673-6", "marketing_start_date": "20240522"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8673-9)", "package_ndc": "68788-8673-9", "marketing_start_date": "20240522"}], "brand_name": "Etodolac", "product_id": "68788-8673_fe4239d0-8003-4b3e-9770-01b21a0dd1d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8673", "generic_name": "Etodolac", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20240522", "listing_expiration_date": "20261231"}