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
68788-8580
Product ID
68788-8580_e2a6b657-7429-4c8a-9a7e-c2ecf679553c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210704
Listing Expiration
2026-12-31
Marketing Start
2024-02-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888580
Hyphenated Format
68788-8580
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
ANDA210704 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (68788-8580-6)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e2a6b657-7429-4c8a-9a7e-c2ecf679553c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["197686"], "spl_set_id": ["da6b2813-a488-4760-90a4-28c67ba3d521"], "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 (68788-8580-6)", "package_ndc": "68788-8580-6", "marketing_start_date": "20240205"}], "brand_name": "Etodolac", "product_id": "68788-8580_e2a6b657-7429-4c8a-9a7e-c2ecf679553c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-8580", "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": "ANDA210704", "marketing_category": "ANDA", "marketing_start_date": "20240205", "listing_expiration_date": "20261231"}