Methocarbamol

Product NDC

70518-1058

11-digit product format

705181058

Labeler code

70518

Product ID

70518-1058_900e861b-cbf8-b37b-e053-2995a90a5cb2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA085159

Marketing category

ANDA

Marketing start

2018-03-13

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