Methocarbamol

Product NDC

63187-369

11-digit product format

631870369

Labeler code

63187

Product ID

63187-369_ad4eb957-585f-4934-b6c4-dfc37dc05c9e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA200958

Marketing category

ANDA

Marketing start

2015-07-13

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

2020-12-31

Current FDA listing

Historical FDA.report record