etodolac
Generic: etodolac
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
etodolac
Generic Name
etodolac
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
etodolac 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-671
Product ID
43063-671_413a0566-5adc-8c09-e063-6294a90a134e
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)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063671
Hyphenated Format
43063-671
Supplemental Identifiers
RxCUI
UPC
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
ANDA076004 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-671-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "413a0566-5adc-8c09-e063-6294a90a134e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0343063671306"], "unii": ["2M36281008"], "rxcui": ["199390"], "spl_set_id": ["41bd86b9-2ef3-49a4-874e-fe8ac6891080"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-671-30)", "package_ndc": "43063-671-30", "marketing_start_date": "20180116"}], "brand_name": "Etodolac", "product_id": "43063-671_413a0566-5adc-8c09-e063-6294a90a134e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43063-671", "generic_name": "Etodolac", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}