Etodolac

Product NDC: 51655-165
11-digit product format: 516550165
Labeler code: 51655
Product ID: 51655-165_76489519-031d-4c8e-a423-a8484eab5730
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Etodolac
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA075074
Marketing category: ANDA
Marketing start: 2014-10-29
Marketing end: 0000-00-00
Substance: ETODOLAC
Active strength: 500 mg/1
Pharmacologic classes: Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag: No
Listing certified through: 2019-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bb9faa76-10d1-4b5f-ab9b-d6a26495edb7	Product name	1	20250311
0c3d95a8-02c3-425e-810b-2a14408d9a06	Product name	4	20250218
24aa5265-325f-0e21-8836-2c9a907c0454	Product name	2	20210601

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-165-52	2026-01-10	C162847	48780-1	9d75b9d0-0cdc-f424-e053-dadaa90a57ce	Etodolac
51655-165-52	2020-01-31	C162847	48780-1	9d75b9d0-0cdc-f424-e053-dadaa90a57ce	Etodolac

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ETODOLAC	ACTIVE INGREDIENT	2M36281008	ETODOLAC TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
ETODOLAC	ACTIVE MOIETY	2M36281008	ETODOLAC TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-165	ETODOLAC TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20141106_aca727e5-435f-4e9b-a049-1a019cf1fa3b.zip