etodolac

Generic: etodolac

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name etodolac
Generic Name etodolac
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

etodolac 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3974
Product ID 50090-3974_a9574834-3e3e-446d-a32d-3fb19d874a75
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)
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 500903974
Hyphenated Format 50090-3974

Supplemental Identifiers

RxCUI
199390
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 ANDA208834 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-3974-0)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-3974-5)
source: ndc

Packages (2)

50090-3974-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-3974-0) 50090-3974-5 60 TABLET, FILM COATED in 1 BOTTLE (50090-3974-5)

Ingredients (1)

etodolac (500 mg/1)

Linked Drug Pages (1)

Etodolac ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a9574834-3e3e-446d-a32d-3fb19d874a75", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["199390"], "spl_set_id": ["31a55fb1-9721-4202-af7d-f06074b03102"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-3974-0)", "package_ndc": "50090-3974-0", "marketing_start_date": "20181213"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-3974-5)", "package_ndc": "50090-3974-5", "marketing_start_date": "20181213"}], "brand_name": "Etodolac", "product_id": "50090-3974_a9574834-3e3e-446d-a32d-3fb19d874a75", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50090-3974", "generic_name": "Etodolac", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etodolac", "active_ingredients": [{"name": "ETODOLAC", "strength": "500 mg/1"}], "application_number": "ANDA208834", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}