Methocarbamol

Product NDC

70518-0431

11-digit product format

705180431

Labeler code

70518

Product ID

70518-0431_5e750a62-7393-0868-e053-2a91aa0a97d2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA040489

Marketing category

ANDA

Marketing start

2017-04-19

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record