etodolac
Generic: etodolac
Labeler: doc rxDrug Facts
Product Profile
Brand Name
etodolac
Generic Name
etodolac
Labeler
doc rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
etodolac 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69306-020
Product ID
69306-020_cd0929e3-c3ce-c89a-e053-2a95a90a7b2a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208834
Listing Expiration
2026-12-31
Marketing Start
2018-06-11
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69306020
Hyphenated Format
69306-020
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
- 20 TABLET, FILM COATED in 1 BOTTLE (69306-020-40)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cd0929e3-c3ce-c89a-e053-2a95a90a7b2a", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["197686"], "spl_set_id": ["cdde46e5-1123-410f-aafc-0c6e904a5d5b"], "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": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (69306-020-40)", "package_ndc": "69306-020-40", "marketing_start_date": "20210616"}], "brand_name": "Etodolac", "product_id": "69306-020_cd0929e3-c3ce-c89a-e053-2a95a90a7b2a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69306-020", "generic_name": "Etodolac", "labeler_name": "Doc Rx", "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": "20180611", "listing_expiration_date": "20261231"}