Metaxalone

Product NDC: 51655-167
11-digit product format: 516550167
Labeler code: 51655
Product ID: 51655-167_3632036c-283f-7194-e054-00144ff8d46c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Metaxalone
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA040445
Marketing category: ANDA
Marketing start: 2016-01-27
Marketing end: 0000-00-00
Substance: METAXALONE
Active strength: 800 mg/1
Pharmacologic classes: Centrally-mediated Muscle Relaxation [PE]
NDC exclude flag: E
Listing certified through: 2017-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-167-20	2026-01-07	C162847	48780-1	9d75b9d0-6d54-f424-e053-dadaa90a57ce	3632036c-283e-7194-e054-00144ff8d46c
51655-167-20	2020-01-31	C162847	48780-1	9d75b9d0-6d54-f424-e053-dadaa90a57ce	3632036c-283e-7194-e054-00144ff8d46c

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-167	METAXALONE TABLET [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20160627_3632036c-283e-7194-e054-00144ff8d46c.zip