Methocarbamol

Product NDC: 51655-141
11-digit product format: 516550141
Labeler code: 51655
Product ID: 51655-141_389f19d2-25dd-40aa-828e-7e0780110109
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Methocarbamol
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA086988
Marketing category: ANDA
Marketing start: 2014-09-23
Marketing end: 0000-00-00
Substance: METHOCARBAMOL
Active strength: 750 mg/1
Pharmacologic classes: Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [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
51655-141-20	2020-01-31	C162847	48780-1	9d75b9d0-cb74-f424-e053-dadaa90a57ce	a5269ffa-a5ad-47c3-a7ff-a05b32add539

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
METHOCARBAMOL	ACTIVE INGREDIENT	125OD7737X	METHOCARBAMOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
METHOCARBAMOL	ACTIVE MOIETY	125OD7737X	METHOCARBAMOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-141	METHOCARBAMOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20140923_a5269ffa-a5ad-47c3-a7ff-a05b32add539.zip