Package 68788-7315-6
Brand: etodolac
Generic: etodolacPackage Facts
Identity
Package NDC
68788-7315-6
Digits Only
6878873156
Product NDC
68788-7315
Description
60 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)
Marketing
Marketing Status
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": "7ad41340-0f91-4093-aceb-e86850c6b585", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["197686"], "spl_set_id": ["55ae2e78-d803-496b-b66d-af1140312785"], "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 (68788-7315-1)", "package_ndc": "68788-7315-1", "marketing_start_date": "20190102"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7315-2)", "package_ndc": "68788-7315-2", "marketing_start_date": "20190102"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7315-3)", "package_ndc": "68788-7315-3", "marketing_start_date": "20190102"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)", "package_ndc": "68788-7315-6", "marketing_start_date": "20190102"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7315-9)", "package_ndc": "68788-7315-9", "marketing_start_date": "20190102"}], "brand_name": "Etodolac", "product_id": "68788-7315_7ad41340-0f91-4093-aceb-e86850c6b585", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-7315", "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": "ANDA208834", "marketing_category": "ANDA", "marketing_start_date": "20190102", "listing_expiration_date": "20261231"}