etodolac
Generic: etodolac
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
etodolac
Generic Name
etodolac
Labeler
bryant ranch prepack
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
etodolac 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1230
Product ID
71335-1230_f91abb0f-25ae-4086-81b9-6d23820e5108
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
713351230
Hyphenated Format
71335-1230
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
- 500 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1230-1)
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1230-2)
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1230-3)
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1230-4)
- 6 TABLET, FILM COATED in 1 BOTTLE (71335-1230-5)
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1230-6)
- 14 TABLET, FILM COATED in 1 BOTTLE (71335-1230-7)
Packages (7)
71335-1230-1
60 TABLET, FILM COATED in 1 BOTTLE (71335-1230-1)
71335-1230-2
90 TABLET, FILM COATED in 1 BOTTLE (71335-1230-2)
71335-1230-3
30 TABLET, FILM COATED in 1 BOTTLE (71335-1230-3)
71335-1230-4
100 TABLET, FILM COATED in 1 BOTTLE (71335-1230-4)
71335-1230-5
6 TABLET, FILM COATED in 1 BOTTLE (71335-1230-5)
71335-1230-6
20 TABLET, FILM COATED in 1 BOTTLE (71335-1230-6)
71335-1230-7
14 TABLET, FILM COATED in 1 BOTTLE (71335-1230-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f91abb0f-25ae-4086-81b9-6d23820e5108", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["2M36281008"], "rxcui": ["199390"], "spl_set_id": ["4b0d1245-8d01-4fff-9783-cb30c17d9246"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1230-1)", "package_ndc": "71335-1230-1", "marketing_start_date": "20190528"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1230-2)", "package_ndc": "71335-1230-2", "marketing_start_date": "20240517"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1230-3)", "package_ndc": "71335-1230-3", "marketing_start_date": "20240517"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1230-4)", "package_ndc": "71335-1230-4", "marketing_start_date": "20240517"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-1230-5)", "package_ndc": "71335-1230-5", "marketing_start_date": "20240517"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1230-6)", "package_ndc": "71335-1230-6", "marketing_start_date": "20240517"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71335-1230-7)", "package_ndc": "71335-1230-7", "marketing_start_date": "20240517"}], "brand_name": "Etodolac", "product_id": "71335-1230_f91abb0f-25ae-4086-81b9-6d23820e5108", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-1230", "generic_name": "Etodolac", "labeler_name": "Bryant Ranch Prepack", "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"}