etodolac
Generic: etodolac
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
etodolac
Generic Name
etodolac
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
etodolac 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7315
Product ID
68788-7315_7ad41340-0f91-4093-aceb-e86850c6b585
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208834
Listing Expiration
2026-12-31
Marketing Start
2019-01-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887315
Hyphenated Format
68788-7315
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
etodolac (source: ndc)
Generic Name
etodolac (source: ndc)
Application Number
ANDA208834 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-7315-1)
- 20 TABLET, FILM COATED in 1 BOTTLE (68788-7315-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-7315-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-7315-9)
Packages (5)
68788-7315-1
100 TABLET, FILM COATED in 1 BOTTLE (68788-7315-1)
68788-7315-2
20 TABLET, FILM COATED in 1 BOTTLE (68788-7315-2)
68788-7315-3
30 TABLET, FILM COATED in 1 BOTTLE (68788-7315-3)
68788-7315-6
60 TABLET, FILM COATED in 1 BOTTLE (68788-7315-6)
68788-7315-9
90 TABLET, FILM COATED in 1 BOTTLE (68788-7315-9)
Ingredients (1)
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"}