Methocarbamol

Product NDC

63739-166

11-digit product format

637390166

Labeler code

63739

Product ID

63739-166_579003b6-ae3e-43a6-838c-3a6db47e3941

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA040489

Marketing category

ANDA

Marketing start

2003-01-29

Marketing end

0000-00-00

Substance

METHOCARBAMOL

Active strength

500 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