Methocarbamol

Product NDC

63629-6852

11-digit product format

636296852

Labeler code

63629

Product ID

63629-6852_f8b66591-140a-48c4-98a3-feb4dc949648

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

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