Methocarbamol

Product NDC

70518-1577

11-digit product format

705181577

Labeler code

70518

Product ID

70518-1577_9477b622-0db0-76fd-e053-2995a90a61ab

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA208507

Marketing category

ANDA

Marketing start

2018-10-23

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

2020-12-31

Current FDA listing

Historical FDA.report record