etodolac

Generic: etodolac

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name etodolac
Generic Name etodolac
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

etodolac 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-467
Product ID 71205-467_5c5cba7e-33d5-4a93-ad61-ceff43cbd79e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076004
Listing Expiration 2026-12-31
Marketing Start 2003-05-01

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205467
Hyphenated Format 71205-467

Supplemental Identifiers

RxCUI
199390
UPC
0371205467609
UNII
2M36281008
NUI
N0000000160 M0001335 N0000175722

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 ANDA076004 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-467-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-467-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-467-90)
source: ndc

Packages (3)

Ingredients (1)

etodolac (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5c5cba7e-33d5-4a93-ad61-ceff43cbd79e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205467609"], "unii": ["2M36281008"], "rxcui": ["199390"], "spl_set_id": ["0c783997-6f2a-45ae-b899-c060c8be468a"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-467-30)", "package_ndc": "71205-467-30", "marketing_start_date": "20200820"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-467-60)", "package_ndc": "71205-467-60", "marketing_start_date": "20200820"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-467-90)", "package_ndc": "71205-467-90", "marketing_start_date": "20200820"}], "brand_name": "Etodolac", "product_id": "71205-467_5c5cba7e-33d5-4a93-ad61-ceff43cbd79e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-467", "generic_name": "Etodolac", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etodolac", "active_ingredients": [{"name": "ETODOLAC", "strength": "500 mg/1"}], "application_number": "ANDA076004", "marketing_category": "ANDA", "marketing_start_date": "20030501", "listing_expiration_date": "20261231"}