Nabumetone

Product NDC: 51655-600
11-digit product format: 516550600
Labeler code: 51655
Product ID: 51655-600_87fa25f6-1665-4327-b5e6-127805754cda
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Nabumetone
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA091083
Marketing category: ANDA
Marketing start: 2014-10-28
Marketing end: 0000-00-00
Substance: NABUMETONE
Active strength: 750 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-600-52	2026-01-06	C162847	48780-1	9d75b9d1-1506-f424-e053-dadaa90a57ce	9845018d-6d10-4414-b94d-f7bd9888ad99
51655-600-52	2020-01-31	C162847	48780-1	9d75b9d1-1506-f424-e053-dadaa90a57ce	9845018d-6d10-4414-b94d-f7bd9888ad99

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
NABUMETONE	ACTIVE INGREDIENT	LW0TIW155Z	NABUMETONE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1
NABUMETONE	ACTIVE MOIETY	LW0TIW155Z	NABUMETONE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-600	NABUMETONE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20141031_9845018d-6d10-4414-b94d-f7bd9888ad99.zip