Package 0093-7172-01

Brand: etodolac

Generic: etodolac
NDC Package

Package Facts

Identity

Package NDC 0093-7172-01
Digits Only 0093717201
Product NDC 0093-7172
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7172-01)

Marketing

Marketing Status
Marketed Since 2000-08-11
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": "05075c98-6f18-44d0-84d4-28d169638e85", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["310245", "310247", "359500"], "spl_set_id": ["f3bf1675-8fda-40d3-8427-0a6a6133a3d3"], "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": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7172-01)", "package_ndc": "0093-7172-01", "marketing_start_date": "20000811"}], "brand_name": "Etodolac", "product_id": "0093-7172_05075c98-6f18-44d0-84d4-28d169638e85", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0093-7172", "generic_name": "Etodolac", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etodolac", "active_ingredients": [{"name": "ETODOLAC", "strength": "500 mg/1"}], "application_number": "ANDA075665", "marketing_category": "ANDA", "marketing_start_date": "20000811", "listing_expiration_date": "20261231"}